As per case facts, Dhanuka Agritech Ltd. (appellant) obtained registration for importing Halosulfuron Methyl (HSM) 75percent WG. Later, Crystal Crop Protection Ltd. (CCPL) secured an RTT Permit for HSMT 98percent ...
LPA 215/2023 Page 1 of 43
$~
* IN THE HIGH COURT OF DELHI AT NEW DELHI
Reserved on: 20 February 2026
Pronounced on: 29 May 2026
+ LPA 215/2023 & CM APPLs. 15489/2023 & 74892/2025
DHANUKA AGRITECH LTD. ....Appellant
Through: Ms. Shoba Ramamoorthy, Mr.
Ankit Virmani and Ms. Devanshi Sharma,
Advs.
versus
UNION OF INDIA THROUGH
THE SECRETARY & ORS. .....Respondents
Through: Mr. Vardhman Kaushik, Adv.,
Mr. Nishant Gautam CGSC, Ms. Kavya
Shukla, Mr. Vineet Negi., Mr. Naman
Sharma, Ms. Theresa, Mr. Vibhav V. Nath
Advs. for UOI
Mr. Arvind Nigam, Sr. Adv. with Mr.
Gaurav Barathi, and Mr. Harsh Gupta, Advs.
for R-4
CORAM:
HON'BLE MR. JUSTICE C. HARI SHANKAR
HON'BLE MR. JUSTICE OM PRAKASH SHUKLA
% JUDGMENT
29.05.2026
C. HARI SHANKAR, J.
A. The lis
1. Consequent to a decision taken in the 349
th
meeting of the
Registration Committee
1
on 9 July 2014, the Directorate of Plant
1
“RC” hereinafter
LPA 215/2023 Page 2 of 43
Protection, Quarantine and Storage
2
granted registration to the
appellant, under Section 9(3)
3
of the Insecticides Act
4
, 1968, for
import of Halosulfuron Methyl
5
75% WG
6
, manufactured by M/s
Nissan Chemical Industries Ltd, Tokyo, Japan and supplied by M/s
Nissei Corporation, Tokyo Japan. The HSM 75% imported by the
appellant is sold by it, in the market, under the trade name “Sempra”.
2. Prior thereto, in 2011, Crystal Crop Protection Ltd
7
applied, in
terms of the “Guidelines for Import of Sample Quantity of Pesticides
for Research, Test and Trial (RTT)
8
Purposes”, approved by the RC in
its 148
th
meeting held on 11 November 1994, 245
th
meeting held on 2
July 2004 and 329
th
meeting held on 8 June 2012, which read thus:
“GUIDELINES FOR IMPORT OF SAMPLE QUANTITY OF
PESTICIDES FOR RESEARCH, TEST AND TRIAL (RTT)
PURPOSES
(As approved by Registration committee in its 148
th
meeting held on 11.11.1994, 245
th
meeting held on
2.7.2004 and 329
th
meeting held on 8.6.2012)
2
“the DPPQS” hereinafter
3
9. Registration of insecticides –
(3) On receipt of any such application for the registration of an insecticide, the Committee
may, after such enquiry as it deems fit and after satisfying itself that the insecticide to which the
application relates conforms to the claims made by the importer or by the manufacturer, as the case
may be, as regards the efficacy of the insecticide and its safety to human beings and animals,
register, on such conditions as may be specified by it and on payment of such fee as may be
prescribed, the insecticide, allot a registration number thereto and issue a certificate of registration
in token thereof within a period of twelve months from the date of receipt of the application:
Provided that the Committee may, if it is unable within the said period to arrive at a
decision on the basis of the materials placed before it, extend the period by a further period not
exceeding six months:
Provided further that if the Committee is of opinion that the precautions claimed by the
applicant as being sufficient to ensure safety to human beings or animals are not such as can be
easily observed or that notwithstanding the observance of such precautions the use of the
insecticide involves serious risk to human beings or animals, it may refuse to register the
insecticide.
4
“the Act” hereinafter
5
“HSM” hereinafter
6
“Water Dispersible Granules”
7
“CCPL” hereinafter
8
“RTT” hereinafter
LPA 215/2023 Page 3 of 43
I. Permission for import of sample quantity of pesticides may
be given by Secretary, CIB&RC for all cases except the following:
i. Pesticides falling under Red Colour toxicity triangle
i.e. extremely toxic category (LD50 value is more than 50
mg/kg body weight).
ii. Coded compounds which are not registered in any
country and do not figure in pesticides manual.
II. Permission issued by Secretary CIB&RC should be brought
to RC for ex-post- facto approval.
III. Documents Requirements for seeking RTT Import permit:
1. Complete Form C (Copy attached).
2. Technical bulletin from inventor/manufacturer.
3. Information on Chemistry, toxicity and bio-efficacy.
4. Justification for quantity.
5. Authenticated copy of the Registration Certificate
for manufacture of particular molecule/pesticide in that
country, issued from the Registration Authority.
6. Authorization for supplier in case of sample
quantity is not supplied by the Manufacturer.
7. For coded & non-registered pesticides authentic
document from the Inventor.”
3. Consequent thereupon, CCPL was granted an RTT Permit for
importing a sample of Halosulfuron Methyl Technical
9
98% w/w
minimum, from Fertiagro, Singapore. The Permit was granted for the
purpose of generating data to be submitted in future for obtaining
registration for importation of HSMT.
9
“HSMT” hereinafter
LPA 215/2023 Page 4 of 43
4. On 11 April 2016, CCPL filed an application under Section 9(3)
of the Act for registration for HSMT 98% min. for permission to
import the product for formulation indigenous manufacture of HSM
75% WG. The application was filed as a “TI – new source”
application. The manufacturer was declared as Jiangsu and the
supplier as Hebei Bestar Commerce & Trade Co. Ltd
10
, Shijiazhuang,
China. The application declared that the manufacture of HSMT 98%
min by Jiangsu had been authorized by the Institute for the Control of
Agrochemicals, Ministry of Agriculture
11
, China and that HSMT 98%
min was registered in China. It was further declared that Jiangsu held
Registration No. PD20132005 issued by the ICAMA for manufacture
of HSMT 98% min, valid till 11 October 2023.
5. CCPL’s application for permission to import HSMT 98% min
was considered by the RC constituted in terms of Section 5(1)
12
of the
Act in its 429
th
Meeting held on 24, 28 and 30 June 2021. The RC
noted that there was a difference in the source of the HSMT 98% for
which CCPL had been granted RTT Permit, which was Fertiagro,
Singapore, and the source of manufacture of the HSMT 98% min as
declared in the Section 9(3) application dated 11 April 2016, which
was Jiangsu. It was decided that CCPL be asked to explain this
discrepancy in the next meeting of the RC.
10
“Hebei” hereinafter
11
“ICAMA” hereinafter
12
5. Registration Committee.—
(1) The Central Government shall constitute a Registration Committee consisting of a
Chairman, and not more than five persons who shall be members of the Board (including the Drugs
Controller, India and the Plant Protection Adviser to the Government of India)—
(i) to register insecticides after scrutinising their formulae and verifying claims
made by the importer or the manufacturer, as the case may be, as regards their efficacy
and safety to human beings and animals; and
(ii) to perform such other functions as are assigned to it by or under this Act.
LPA 215/2023 Page 5 of 43
6. On 16 July 2021, the appellant addressed a detailed
representation objecting to the application of CCPL for registration of
HSMT 98% min as TI (New Source) and HSM 75% WG as FIM v.
FI, under Section 9(3) of the Act. It was pointed out that the
applications claimed equivalence with the appellant’s registered HSM
and that, therefore, any adverse effect of the product which CCPL
desired to import or indigenously manufacture would directly affect
the appellant as well as the credibility of the HSM molecule itself.
Moreover, submitted the appellant, an untested insecticide could have
widespread adverse effects on public health, safety and the
environment. Expressing alarm at the discrepancy between the source
of import of the HSMT in the Section 9(3) application of CCPL and
the source of import of the HSMT imported under the RTT Permit, the
appellant pointed out that the result was that CCPL had generated data
relating to toxicity and bioefficacy, among other things, of the HSMT
manufactured at one source and was seeking to use the said data to
justify import from another source under Section 9(3) of the Act.
Import registration, submitted the appellant, was source-specific, and
it was but natural that the same product manufactured at different
facilities would have differences, even in respect of purity profile.
This, in turn, could significantly impact the toxicity of the product.
The data generated by a Section 9(3) applicant, on the basis of which
he sought registration, had to be on the product manufactured at the
source from which the applicant desired to import the insecticide. It
was for this reason, submitted the appellant, that the RC, in its 325
th
Meeting on 4 January 2012, required an endorsement of additional
manufacturing site with five batch analytical data from both
LPA 215/2023 Page 6 of 43
manufacturing sites. Accordingly, the appellant requested that the
Section 9(3) applications of CCPL be rejected.
7. In this context, it is relevant to mention that, in its 325
th
Meeting held on 4 January 2012, the RC accepted the
recommendation of the Expert Committee regarding the protocol to be
followed in the event of inclusion, in the registration for import of
insecticides under Section 9(3), of an additional manufacturing site of
the imported insecticides, for incorporation of the following
guidelines:
“(i) The site, proposed to be additional manufacturing site,
should belong to the same registrant (it is not allowed on anyone
else's premises, whatsoever);
(ii) the registrant should have registration for manufacture of
the same insecticide/product in the country where the additional
site is located;
(iii) Letter of consent from already approved source and from
new manufacturing site duly certified by the Designated National
Authority (DNA), which shall be verifiable by the DNA of India:
(iv) Additional declaration from already approved
source/principals as well as from new manufacturing site with
respect to the formulation being made by using technical same raw
material & process from the source which is already approved by
the RC in India;
(v) all operations involved in the manufacturing of the
insecticide for which the additional site is being considered should
be fully operated by the same. registrant and have the proof of
manufacturing there by submitting an undertaking to this effect,
duly certified by the DNA of that country;
(vi) the registrant shall be responsible for manufacturing the
product having identical chemical composition and specifications
as that of the original registered source of the product;
LPA 215/2023 Page 7 of 43
(vii) five batch analytical test report shall be submitted along
with the application for the five batches manufactured at the source
originally registered and the five batches manufactured at the
proposed additional source;
(viii) samples of all the five batch manufactured at the source
originally registered and all the five batches manufactured at the
proposed additional source shall be submitted along with the
respective reference standards to the Sectt of CIB & RC for testing
at CIL for verification;
(ix) the samples and the reference standards should be valid at
least for a period of six month from the date of delivery to the Sectt
of CIB & RC;
(x) documents supporting the claim of the registrant about the
additional manufacturing site, duly certified by the Designated
National Authority (like. ICAMA for China), shall be submitted
along with the application, which shall in turn be verified by the
DNA of India before considering the endorsement;
(xi) intimation about the import of every consignment,
proposed to be imported from the additional manufacturing site,
shall be given to the Sectt of CIB along with the name of the port
of entry into India and expected date of arrival as soon as the
consignment is dispatched from the additional manufacturing site
for arranging the testing of sample(s), if so considered necessary;
(xii) Justification for approval of additional manufacturing site; and
(xiii) failure to meeting any of the above mentioned criteria shall
unconditionally empower the Registration Committee to reject
application for such endorsement; or endorsement, if already
granted.”
8. The explanation proffered by CCPL for the difference in the
source of manufacture of the HSMT between the source reflected in
the RTT permit and the source declared in its Section 9(3) application
dated 11 April 2016 was considered in Agenda Item 2.1 of the 430
th
meeting of the RC, held on 23 July 2021, which read thus:
2.1 Presentation by M/s Crystal Crop Protection Pvt. Ltd., for
grant of registration for indigenous manufacture of
LPA 215/2023 Page 8 of 43
Halosulfuron methyl 75% WG u/s 9(3) FIM vs FI and for
technical import of Halosulfuron methyl technical 98%
w/w min. u/s 9(3).
The presentation was made by the applicant and
submitted the following details:-
1. That they have procured RTT permit for import of
Halosulfuron-Methyl Technical from M/s Fertisgro Ptv
Ltd., 30 Toh Guan Road, #07-06 ODC Districcentre,
Singapore 608 840. Subsequently, the technical Grade
Sample was imported from M/s Fertiagro Pvt. Ltd. The
data for all the disciplines was generated using the said
sample. They also informed that technical grade material
supplied to them by M/s Fertiagro was actually
manufactured by M/s Jiangsu Agrochem Laboratory Co.
ltd., Minjian Road, Hi-tech Zone of Changzhou, Jiangsu,
China with whom they had an exclusive business
agreement for manufacturing and supply of the product.
2. Submitted all the required data in each discipline
according to the guidelines of TI -New Source.
3. Filed an appeal before the Hon'ble Appellate
Authority vide appeal no. 15 & 12 of 2020 and after
hearing case the Appellate authority noted that all
scientific facts and complete data according to the
existing guidelines of TI-New Source have been given
and passed the order vide F. No. 13031/12/2020/PP-1
dated 02/12/2020.
4. Appellate authority was also satisfied, and hence
directed the RC to duly consider the application of
Technical of the Product HALOSULFURON TECH 98%
Min for import from another new source.
5. Further informed that Registration Committee in
its 369th Meeting held on 04.10.2016, vide Agenda Item
No. 2.2 taken decision that "The committee further
decided that no application with the data generated using
unauthorized sample (without obtaining RTT permit)
shall be accepted/processed on or after 01/01/2017. It was
also decided that if any studies of any product under any
category is undergoing with such samples, the same may
be intimated to the APPA & Secretary (CIB&RC) by
30/11/2016 through email at cibsecy@nic.in. A Public
Notice to this effect was also issued".
6. Applicant appraised that they submitted a letter to
LPA 215/2023 Page 9 of 43
Secretary CIB&RC on 03/11/2016 (within the deadline
indicated) informing the reason and change in the name
of source import.
7. It was also noticed that applicant submitted the
dossier with revised Form 1 dated 11.4.2016 received in
CIBRC Secretariat on 22.4.2016 where the applicant
indicated original manufacturer Jiangsu Agrochem Lab
Co. Ltd.
RC deliberated the agenda and after consideration of
point number 5 of 369th RC and also point number 6 and
7, found that this case qualifies for registration u/s 9(3).
Accordingly granted for registration for indigenous
manufacture of Halosulfuron methyl 75% WG for control
of Cyperus rotundus on Sugarcane; Cyperus rotundus
Cyperus iria on Maize and Cyperus rotundus, Cyperus
iria on Bottle Gourd in the category FIM vs FI and for
technical import of Halosulfuron methyl technical 98%
w/w min. manufactured by M/s Jiangsu Agrochem
Laboratory Co. Ltd., Minjiang Road, Hi-tech Zone of
Changzhou, Jingsu, China through supplier M/s Hebei
Bestar commerce and Trade Co. Ltd., No. 6-3-203, No.
66, Dianda Street Xinhua District Shijiazhuang, China
with validity 11.10.2023.
Thus, the RC decided, after examining the presentation and
explanation proffered by CCPL for the difference in the source of the
HSMT between the RTT sample and the product for which import
registration was sought, to grant registration, to CCPL, both for
indigenous manufacture of HSM 75% WG in the FIM v. FI
13
category
and for Technical Import of HSMT 98% w/w min, manufactured by
Jiangsu and supplied by Hebei.
9. At this juncture, it would be relevant to reproduce the
Guidelines issued by the RC governing FIM v. FI category imports, in
13
Formulation Indigenous Manufacture v Formulation Import
LPA 215/2023 Page 10 of 43
exercise of the powers conferred by Section 5(5)
14
of the Act read
with Rule 4(b)
15
of the Insecticides Rules, 1971, thus:
Guidelines applicable to FIM v. FI imports as approved in 315
th
meeting of the RC held on 22 February 2011
“The Guidelines for the category of FIM Vs. Fl are as under:-
(a) For registration of pesticide formulation for
indigenous manufacture having the identical chemical
composition that of formulation already registered for
import U/s.9(3).
No data is required provided the technical of the
source to be used in formulation is duly registered
as per guidelines of the Registration Committee and
the label claims are same.
(b) For registration of pesticide formulation for
indigenous manufacture having the different chemical
composition that of formulation already registered for
import U/s.9(3).
Complete data to be submitted as per already
existing guidelines for formulation indigenous
manufacture (FIM) U/s. 9(3) provided the technical
(source) to be used for making formulation is duly
registered as per guidelines of the Registration
Committee.”
10. In the 431
st
RC meeting held on 27 August 2021, vide Agenda
Item No. 1.0, the minutes of the 430
th
RC meeting were confirmed
with a modification in Agenda Item 2.1 by inserting a final paragraph
which read:
14
(5) The Registration Committee shall regulate its own procedure and the conduct of business to be
transacted by it.
15
4. Functions of Registration Committee.—The Registration Committee shall, in addition to the functions
assigned to it by the Act, perform the following functions, namely:—
*****
(b) carry out such other incidental or consequential matters necessary for carrying out the
functions assigned to it under the Act or these rules.
LPA 215/2023 Page 11 of 43
“An affidavit on NJSP should be submitted to support the
requirement of an agreement between M/s Fertiagro Pvt Ltd, 30
Toh Guan Road, #07-06 ODC Districcentre, Singapore 608 840
and M/s Jiangsu Agrochem Laboratory Co. Ltd, Minjian Road, Hi-
tech Zone of Changzhou, Jingisan China to establish the linkage
for using the same technology and same manufacturing process as
was used for supply of RTT sample.”
11. CCPL, in terms of the above directions, filed an affidavit dated
8 September 2021 with the RC enclosing, therewith, the following
letter dated 10 August 2021 issued by Jiangsu:
“We, JIANGSU AGROCHEM LABORATORY CO. LTD. ADD
:Minjiang Road. Hi-tech Zone of Changzhou, Jiangsu, China,
hereby confirm the following:
1. Jiangsu Agrochem Laboratory Co., Ltd, established in Apr
1999, located in National High-tech Industrial Development Zone
of Changzhou, Jiangsu Province, is the Provincial Engineering
Center as well as Provincial Hi-tech Enterprise approved by the
Provincial Council of Science and Technology.
2. It's been listed as development base of herbicides with high
efficiency by Ministry of Science and Technology of P.R.C.
3. We further confirm that we hold valid registration of
Halosulfuron Methyl Technical min issued by INSTITUTE OF
THE CONTROL OF AGROCHEMICALS,’ Ministry of
Agriculture (ICAMA) having registration reference number
PD20132005. We had received this registration first time in the
year 2013. We had received a temporary registration from ICAMA
in 2011 vide registration number LS20110312. A copy of the same
is also enclosed and can be found on ICAMA website.
4. We further confirm that we are the only manufacturer who
has a valid ICAMA for Halosulfuron Methyl Technical in China.
5. We also confirm that we are the only legal manufacturer of
Halosulfuron Methyl Technical 98% min in China. Our latest
manufacturing license number is 0086 issued by Department of
Agriculture and Rural Development of Jiangsu Province dated 03
April 2018. We are producing this product in China since the year
2011.
LPA 215/2023 Page 12 of 43
6. We also confirm that we had provided technical grade
sample to M/s, Fertiagro Pte, Singapore between 2010-2014. The
purpose of the sample was to support registration in India for our
customer M/s. Crystal Crop Protection Ltd. (Earlier known as
Crystal Crop Protection Pvt. Ltd.). We later sent tech grade
samples to Crystal directly also for registration related purposes.”
12. On 6 August 2021, the appellant submitted a petition,
purportedly under Sections 10
16
and 11
17
of the Act, challenging the
grant of registration to CCPL for import and indigenous manufacture
of HSMT/HSM WG. The appellant submitted that registration had
been granted to CCPL without any verification of its claim that the
RTT sample had been manufactured by Jiangsu. Import of pesticide
for indigenous use, or for use in indigenous manufacture of pesticide,
from a source other than that from which the sample in respect of
which the test data had been provided by the Section 9(3) applicant, it
was submitted, was not permissible.
13. By order dated 10 September 2021, the Joint Secretary (Plant
Protection), in his capacity of Revisionary Authority, rejected the
petition submitted by the appellant. The Revisionary Authority held
the petition not to be maintainable as an appeal under Section 10 and
16
10. Appeal against non-registration or cancellation.—Any person aggrieved by a decision of the
Registration Committee under Section 9 may, within a period of thirty days from the date on which the
decision is communicated to him, appeal in the prescribed manner and on payment of the prescribed fee to
the Central Government whose decision thereon shall be final:
Provided that the Central Government may entertain an appeal after the expiry of the said period, if
it is satisfied that the appellant was prevented by sufficient cause from filing the appeal in time.
17
11. Power of revision of Central Government.— The Central Government may, at any time, call for
the record relating to any case in which the Registration Committee has given a decision under Section 9 for
the purpose of satisfying itself as to the legality or propriety of any such decision and may pass any such
order in relation thereto as it thinks fit:
Provided that no such order shall be passed after the expiry of one year from the date of the
decision:
Provided further that the Central Government shall not pass any order prejudicial to any person
unless that person has had a reasonable opportunity of showing cause against the proposed order.
LPA 215/2023 Page 13 of 43
rejected it on merits under Section 11. The reasoning and conclusion
in the said order dated 10 September 2021 read thus:
“Now after going through the contents of the appeal/revision
petition and after hearing the oral and written submissions
advanced by the respective parties, I am of the view that as far as
maintainability of the appeal is concerned, Section 10 of the Act
deals with 'Appeal against non-registration or cancellation' and that
legal remedy in this case is circumscribed by condition of non-
registration or cancellation. The contention raised by the
appellant/revisionist pertains to the grant of registration of
Halosulfuron methyl Technical 98% min to the respondent No 2
(third party) and that, it the grant of registration that has been
challenged and not the non-registration or cancellation and
therefore does not fall in the ambit of the Section 10 of the Act.
Therefore, the appeal is not maintainable.
Further, as far as power of revision of Central Government
as envisaged in Section 11 of the Insecticides Act, in the instant
case, appellant/ revisionist has not provided any documentary
evidence to prove that decision of RC is perverse or mala fide and
that respondents have not followed the guidelines issued by
CIBRC or has not completed the process of registration with
respect to submission of data for evaluation of safety and efficacy
of the product in question. Therefore, I am of the view that,
revision petition is not maintainable.
In view of the above, I further observe that according to the
minutes of 430th RC meeting, Registration Committee after
reviewing all the facts and information as per guidelines, had fully
satisfied itself with regard to the data submitted by the applicant
before granting the approval for registration for import of
Halosulfuron Technical 98% min from the said source. Thus, I am
of the view that the decision given by the RC is justified and
require no interference from this appellate authority.”
14. Aggrieved thereby, the appellant approached this Court by
means of WP (C) 10776/2021, which stands dismissed by a learned
Single Judge of this Court.
15. This appeal challenges the said decision.
LPA 215/2023 Page 14 of 43
B. The Impugned Judgment
I. Rival Contentions
IA Contentions of the appellant
16. The appellant submitted, before the learned Single Judge, that
Jiangsu had been granted registration, by the registering authorities in
China, for manufacture of 98% HSM only on 11 October 2018 and
that, therefore, CCPL could not have declared Jiangsu to be its source
of manufacture of the HSMT in 2016. Besides, the Guidelines issued
by the RC required that, if the manufacturer of the imported pesticide,
and the supplier from whom it was being sourced, were different, both
names had to figure on the RTT Permit, which had not been complied
with. Inviting attention to the Statement of Objects and Reasons of the
Act, the appellant submitted that there had been complete abdication,
by the RC, of its duty under Section 9(3).
17. In such circumstances, the appellant submitted that the
appeal/revision petition preferred by it before the Revisionary
Authority was maintainable and that the words “person aggrieved”, as
employed in Section 10 of the Act were required to be widely
construed, keeping in mind the Statement of Objects and Reasons of
the Act and considerations of larger public interest. Public interest, it
was submitted, would irremediably jeopardised if CCPL were to be
permitted to import pesticide from an untested source. Use of such
pesticides could jeopardise the life and safety of humans and animals
LPA 215/2023 Page 15 of 43
and also adversely impact the environment. It was imperative,
therefore, that the import, under Section 9(3), took place from the
same source from which the sample, which was earlier tested and with
respect to which data was generated, was manufactured. The appellant
submitted that the affidavit of CCPL, as was directed to be filed in the
431
st
RC Meeting, would not be any panacea, as it would obviously be
self-serving in nature.
18. In so far as appellant’s locus was concerned, it was further
submitted that, as, while applying for registration of HSM under the
“TI (new source)” category, equivalence had been claimed, by CCPL,
with the HSM earlier imported by the appellant. As such, if the HSMT
imported by CCPL did not function properly, or caused any adverse
effects, it would damage the appellant’s reputation and also jeopardise
the reputation of the HSM molecule itself. In support of its contention
that it possessed locus, the appellant placed reliance on the judgments
of the Supreme Court in Coal India Ltd v. Ananta Saha
18
, Samir
Agrawal v. Competition Commission of India
19
and Honnaiah T.H.
v. State of Karnataka
20
.
IB. Contentions of CCPL
19. CCPL submitted, by way of response, that the challenge, by the
appellant, to the grant of registration to CCPL under Section 9(3) of
the Act was lacking in bona fides, and that the appellant wanted to
perpetrate its monopoly with respect to import of HSM. In any event,
18
(2011) 5 SCC 142
19
(2021) 3 SCC 136
20
2022 SCC OnLine SC 1001
LPA 215/2023 Page 16 of 43
submitted CCPL, the appellant had no locus standi to maintain its
challenge, and was merely a meddlesome interloper. The appellant’s
revision petition/appeal was not maintainable under Section 10 of the
Act, as a challenge, under the said provision, lay only against a
decision refusing registration or cancelling a registration and not
against grant of a registration. The appellant, it was submitted, could
not be said to be a “person aggrieved”, as the appellant was not
affected by grant of registration to CCPL.
20. Besides, submitted CCPL, registration had been granted to
CCPL after complete scrutiny of its application, which was containing
all requesite details for the period 2016 to 2021. Such a decision, it
was submitted, would ordinarily not be subject to judicial review.
21. To support its contentions, CCPL relied on the judgments of the
Supreme Court in Uflex Ltd v. Government of Tamil Nadu
21
and
Jasbhai Motibhai Desai v. Roshan Kumar
22
and the judgments of
this Court in Syngenta India Ltd v. Union of India
23
and Gharda
Chemicals Ltd v. Joint Secretary
24
.
II. Analysis by the learned Single Judge
22. The learned Single Judge, at the outset, identified the bone of
contention, before him, as being the legality of the registration granted
21
2021 SCC OnLine SC 861
22
(1976) 1 SCC 671
23
2009 SCC OnLine Del 1724
24
Judgment dated 26 October 2018 in WP (C) 11542/2018
LPA 215/2023 Page 17 of 43
to CCPL by the RC in its 430
th
meeting, for import and manufacture
of HSMT.
23. The learned Single Judge reasoned as under:
“22. Perusal of the record reveals that Jiangsu, China was the
authorized manufacturer of Halosulfuron Methyl Technical 98 %
min since 2011. In the year, 2011, Jiangsu, China had received a
temporary registration of Halosulfuron Methyl Technical 98 %
from ICAMA vide registration number LS2011031. The said
registration of Jiangsu for Halosulfuron Methyl Technical 98 %
min was subsequently granted permanent registration number by
ICAMA in the year 2013 vide registration number PD20132005.
Perusal of the record further reveals that an Agreement dated
08.12.2010 was executed between M/s Jiangsu Agrochem
Laboratory Co. Ltd. and M/s. Fertiagro Pte Ltd. for supply of
material. It was agreed between the parties that since M/s Fertiagro
Pte Ltd. had a good distribution network, and M/s Jiangsu
Agrochem Laboratory Co. Ltd. being a manufacturer of agro-
chemicals, the latter would supply the goods to M/s Fertiagro Pte
Ltd. for further sale as its distributor/agent. It was agreed that M/s.
Fertiagro Pte Ltd. may send the product to its customers for
registration in respective territory and in case the product is
registered in respective country, M/s Jiangsu Agrochem
Laboratory Co. Ltd. shall continue to supply product through M/s
Fertiagro Pte Ltd.
23. Learned senior counsel for the Petitioner further contended
that Respondent no. 4 failed to comply with the guidelines
provided by the RC which mandates that in case the manufacturer
was different from supplier, the details of both were required to be
mentioned on the RTT Permit. Perusal of the file reveals that the
new guidelines came into effect vide 329
th
RC Meeting held on
08.06.2012; whereas the RTT permit to Respondent No. 4 was
issued in the year 2011. Hence Respondent No. 4 applied for the
RTT permit as per the old guidelines in which there was no such
requirement. Further, perusal of the record reveals that the
Registration Committee in its 369
th
Meeting held on 04.10.2016,
vide Agenda Item No. 2.2 took a decision that ‘no application with
the data generated using unauthorized sample (without obtaining
RTT permit) shall be accepted/processed on or after 01/01/2017. It
was also decided that if any studies of any product under any
category is undergoing with such samples, the same may be
intimated to the APPA & Secretary (CIB&RC) by 30/11/2016
LPA 215/2023 Page 18 of 43
through email at cibsecy@nic.in. A Public Notice to this effect was
also issued’. Taking benefit of the said decision, Respondent No. 4
vide letter dated 03.11.2016 appraised the Secretary CIB & RC of
the reason and change in the name of source import. Respondent
No. 4 further submitted a dossier with revised Form 1 dated
11.04.2016 in which Respondent No. 4 indicated the original
manufacturer as M/s Jiangsu Agrochem Laboratory Co. Ltd.
24. This Court has examined the minutes of 430
th
meeting of
the RC wherein the RC has recorded the history of the dossiers and
other relevant data submitted by Respondent no. 4. The relevant
portions of the said RC Meeting, reads, inter alia, as follows
25
:
*****
25. Apart from that, Respondent no. 4 has submitted before the
RC time and again such documentary evidences to establish link
between the M/s Fertiagro, Singapore and M/s Jiangsu Agrochem
Laboratory, China.
26. This Court also finds that the RC vide item No. 1.0 of its
431
st
meeting dated 27.08.2021 directed Respondent no. 4 to
submit an affidavit to support the requirement of an agreement
between Fertiagro and Jiangsu to establish the linkage for using the
same technology and same manufacturing process as was used for
supply of RTT sample. In view of the same, Respondent no. 4
submitted the requisite affidavit before the RC along with relevant
documents which includes a letter dated 10.08.2021 from M/s
Jiangsu Agrochem Laboratory Company Ltd. The said Letter,
reads, inter alia, as follows
26
:
*****
27. Upon perusal of these documents, it is amply conveyed that
RC had sufficient material before it to satisfy itself with respect to
the claims made by Respondent no. 4.
28. At this point, it is relevant to refer to the provision under
Section 9(3) of the Act. It is reproduced as follows:
“(3) On receipt of any such application for the
registration of an insecticide, the Committee may, after
such enquiry as it deems fit and after satisfying itself that
the insecticide to which the application relates conforms to
the claims made by the importer or by the manufacturer, as
the case may be, as regards the efficacy of the insecticide
25
Already extracted in para 8 supra
26
Already reproduced in para 11 supra
LPA 215/2023 Page 19 of 43
and its safety to human beings and animals, register [on
such conditions as may be specified by it] and on payment
of such fee as may be prescribed, the insecticide, allot a
registration number thereto and issue a certificate of
registration in token thereof within a period of twelve
months from the date of receipt of the application:
Provided that the Committee may, if it is unable
within the said period to arrive at a decision on the basis of
the materials placed before it, extend the period by a further
period not exceeding six months:
Provided further that if the Committee is of opinion
that the precautions claimed by the applicant as being
sufficient to ensure safety to human beings or animals are
not such as can be easily observed or that notwithstanding
the observance of such precautions the use of the
insecticide involves serious risk to human beings or
animals, it may refuse to register the insecticide.”
29. On the bare perusal of the aforesaid provision, it is cogent
that liberty/discretion has been granted to the RC to conduct its
affair or enquiry as it deems fit for ascertaining the claims of the
applicant.
30. While examining the decision of an expert quasi-judicial
body under Article 226 of the Constitution of India, the High Court
is concerned only to the limited extent whether the said authority
has applied its mind and satisfied itself with help of relevant data,
so that no room is left for arbitrariness. This Court is convinced
that RC indeed took all the possible steps to check the veracity of
the registration application and mindfully granted registration
under the statute.
31. The Petitioner has not brought on record any documentary
evidence to prove that the decision of RC suffers from irregularity
or that it has proceeded arbitrarily while satisfying itself with
respect to efficacy and safety of the product in question. RC is a
body of experts comprising of experts from various fields. RC
comprises of authority such as Drugs Controller of India and the
Plant Protection Advisor to the Government of India etc. The
Court cannot interfere with the decisions taken by the RC by
exercising power of judicial review unless and until it suffers from
patent irregularity. Same observations were made by co-ordinate
Bench of this Court in Crop Care Federation of India v. UOI in
W.P. (C) 8117/2019 decided on 29.07.2019.
LPA 215/2023 Page 20 of 43
32. As far as maintainability of the appeal under Section 10 of
the Act is concerned, it is explicitly provided in the provision that
only a ‘person aggrieved’ can prefer an appeal against the decision
of the RC. The present case is squarely covered by the order
passed by the coordinate Bench of this court in Gharda
Chemicals (supra) wherein the petitioner who happened to be a
competitor of the Respondent, filed a writ petition against the grant
of registration to the Respondent under the Act. Relevant portion
of the aforesaid order is as follow:
“10. This Court is unable to accept that the petitioner has
any vested right to insist that respondent nos 4 and 5's
applications be considered as per any particular guidelines,
and the same requires to be protected by this court by
issuing a writ under Article 226 of the Constitution of
India. Concededly, the applications filed by the petitioner
for registration of insecticides has been processed and the
petitioner now seeks to challenge the processing of
applications of its competitors (respondent nos. 4 and 5).
Plainly, the provisions of Article 226 cannot be permitted
to be used for settling business rivalries, which appears to
be the object of the present petition.
11. In Nagar Rice & Flour Mills v. N Teekappa
Gowda & Bros
27
, the Supreme Court held that a rice mill
owner had no locus standi to challenge setting up of a new
rice mill by another, under Article 226, even if the same
was in contravention of section 8(3)(c) of the Rice Milling
Industry (Regulation) Act, 1958. The Court reasoned that
no right vested in such an applicant was infringed. This
decision was also followed by the Supreme Court in a later
decision in Mithilesh garg v. Union of India
28
, wherein the
court repelled the challenge of existing stage carriage
operators to the decision of the Regional Transport
Authority to issue permits to new operators.
12. In Simbhaoli Sugar Mills v. Union of India
29
a
Division Bench of this court rejected the challenge to a
press note containing guidelines for issuance of licences for
setting up new and expansion of existing sugar factories. In
terms of the said guidelines, licence to set up a new unit
could be granted subject to certain conditions, one of them
being that there was no sugar mill within a radius of fifteen
kilometres and the applicant was not required to furnish
27
(1970) 1 SCC 575
28
(1992) 1 SCC 168
29
(1992) 22 DRJ 594
LPA 215/2023 Page 21 of 43
any certificate/clearance regarding cane availability or
potential for development of cane. The petitioner before the
court was an existing manufacturer and had challenged the
issue of licence to another unit (respondent no. 5 therein)
processed under the guidelines. The court held that the
petitioner had “no locus standi to invoke the special
jurisdiction under Article 226 of the Constitution of India”
and rejected the petition.”
33. It is a well-settled principle that Article 226 of
the Constitution cannot become a means to chase down a business
rival by pinpointing procedural deficiency in decision making
process. This extraordinary power can only be invoked when there
appears a glaring error and arbitrariness in decision making
process of the body. Competition between enterprises cannot be a
cause of action in any case. The Hon'ble Supreme Court touched
upon the issue of locus standi in Jasbhai Motibhai Desai
case (supra):
“47. Thus, in substance, the appellant's stand is that the
setting up of a rival cinema house in the town will
adversely affect his monopolistic commercial interest,
causing pecuniary harm and loss of business from
competition. Such harm or loss is not wrongful in the eye
of law, because it does not result in injury to a legal right or
a legally protected interest, the business competition
causing it being a lawful activity. Juridically, harm of this
description is called damnum sine injuria, the term injuria
being here used in its true sense of an act contrary to
law. [Salmond on Jurisprudence, 12
th
Edn. by Fitzgerald, p.
357, para 85] The reason why the law suffers a person
knowingly to inflict harm of this description on another,
without holding him accountable for it, is that such harm
done to an individual is a gain to society at large.
48. In the light of the above discussion, it is
demonstrably clear that the appellant has not been denied
or deprived of a legal right. He has not sustained injury to
any legally protected interest. In fact, the impugned order
does not operate as a decision against him, much less does
it wrongfully affect his title to something. He has not been
subjected to a legal wrong. He has suffered no legal
grievance. He has no legal peg for a justiciable claim to
hang on. Therefore he is not a “person aggrieved” and has
no locus standi to challenge the grant of the no-objection
certificate.”
LPA 215/2023 Page 22 of 43
34. In the light of aforesaid discussion, this Court holds that the
RC has well-satisfied itself with regard to the bio-efficacy data and
other relevant documents provided by Respondent no. 4 to support
its case for registration under the Act.
35. This Court finds no infirmity or perversity in the impugned
order. No interference with the decision and order impugned in this
petition is warranted at the instance of the petitioner.”
C. Relevant Proceedings before this Court
24. On 1 October 2025, the UOI filed a Brief Note, annexing,
therewith, certain documents. In the said Note, it is stated, with
respect to the RTT Permit which had originally been issued to CCPL,
and with respect to Form C which had been submitted by CCPL for
obtaining the said RTT Permit, as under:
“30.3.2011
RTT issued to Respondent No. 4
The Form C requires the applicant to mention the name of the
source/manufacturer and supplier which in the present matter is
M/s Fertiagro Pvt Ltd, Singapore. The Respondent No. 4 mentioned
the manufacturer and supplier both as M/s Fertiagro Pvt Ltd,
Singapore.”
(Emphasis supplied)
25. During the course of these proceedings, the following order was
passed by this Court on 9 October 2025:
“1. Heard learned Counsels for the Parties in detail.
2. The Union of India i.e. the Respondent No.1 herein, is
directed to produce the relevant documents to demonstrate that M/s
Jiangsu Agrochem Laboratory Co. Ltd. had the temporary
Registration to manufacture Halosulfuron Methyl 98% weight-in-
weight (w/w) from Institute for the Control of Agrochemicals,
LPA 215/2023 Page 23 of 43
Ministry of Agriculture ("ICAMA") vide Registration No.
LS20110312 in the year 2011.
3. Though certain documents have also been given to show
that M/s Jiangsu Agrochem Laboratory Co. Ltd. had the license to
manufacture Halosulfuron Methyl at 95% w/w purity, liberty is
also given to the Respondents to satisfy the Court that a person
having a registration license for manufacturing Halosulfuron
Methyl at 95% w/w can also manufacture the same at 98% w/w.”
There has been no compliance, by the UOI, with the above directions.
26. Following this, the appellant filed CM 74892/2025, praying that
the present appeal be allowed, in view of (i) the disclosure, in the
Brief Note filed by the UOI on 1 October 2025, of the fact that, in the
Form C submitted by CCPL for obtaining the RTT Permit in 2011,
CCPL had mentioned Fertiagro as the manufacturer as well as the
supplier of the HSMT 98% sample, and (ii) the UOI had failed to
comply with the directions, in the order dated 9 October 2025, to
place documents on record to indicate that, in 2011, Jiangsu had the
registration to manufacture HSMT 98%.
D. Rival Contentions before us
I. Submissions of Ms. Shobha Ramamoorthy for the appellant
27. Arguing for the appellant, Ms. Ramamoorthy submits as under:
(i) The impugned registrations, granted to CCPL, permitted
import of HSMT from an untested source. CCPL had, in 2011,
applied for grant of Registration Certificate for import of
LPA 215/2023 Page 24 of 43
sample for research, test and trial. Pursuant to the application,
RTT Permit was issued to CCPL for import of HSMT 98% w/w
from Fertiagro. It was the RTT Sample imported by CCPL
under the said registration which was subjected to trial and test,
and the data generated as a result of which was submitted by
CCPL to the RC for obtaining registration under Section 9(3) of
the Act. Having thus provided data following trial and test
conducted on a sample sourced from Fertiagro, CCPL applied,
under Section 9(3), for grant of registration for import and for
indigenous manufacture of HSM with a new manufacturer, i.e.
Jiangsu and sent by Hebei. After having, in its 429
th
Meeting
conducted on 24
th
June, 28
th
June and 30 June 2021, called upon
CCPL to explain, in the next Meeting of the RC, the
discrepancy between the source of the pesticide, the RC, in the
430
th
meeting conducted on 23 July 2021, blindly accepted the
explanation proffered by CCPL, without any proof or evidence.
All that the RC required of CCPL was the furnishing of an
affidavit, which was obviously self-serving in nature and would
not satisfy the requirement of a proper enquiry into the
discrepancy in source between the RTT Sample and the HSM
which was being proposed to be important and used in the
indigenous manufacture of HSM 75% WG. In fact, the very
calling upon CCPL, by the RC, to file an affidavit, in the 431
st
meeting of the RC on 27 August 2021, indicated that
registration had been granted to CCPL in the 430
th
meeting
without the RC satisfying itself regarding the veracity of the
explanation proffered by CCPL for the discrepancy in the
LPA 215/2023 Page 25 of 43
source of the HSMT between the RTT Sample and the imports
for which application had been made under Section 9(3). The
counter-affidavit filed by the official Respondents, too, did not
indicate any application of mind, by the RC, to the correctness
of the explanation proffered by CCPL in the 430
th
meeting for
the discrepancy in source of the imported HSMT between the
RTT Sample and the proposed Section 9(3) import.
(ii) Jiangsu had been granted registration, in China, for
manufacture of HSMT 98% only on 11 October 2018. Reliance
was placed on the following tabular data, available on the
website of the ICAMA:
Registered info
Registered number: PD20132005 First
Prove:
Oct
11,
2018
Period: Oct 11,
2023
ProductName: Halosulfuron-
methyl 98%
Toxicity: L
Formulation:
TC
Manufacturer: JIANGSU AGROCHEM
LABORATORY CO.LTD.
Country:
Remarks:
ActiveIngredient
ActiveIngredient Content
Halosulfuron-methyl 98%
Jiangsu could not, therefore have been the manufacturer of the
RTT Sample which was imported in 2011. This itself indicated
the falsity of CCPL’s claims. Though it was averred that
Jiangsu had been granted provisional registration for
manufacture of HSMT in 2011, no documents to that effect
were on record, except a self-serving letter from Jiangsu,
extracted in para 11 supra. Moreover, the Guidelines issued by
LPA 215/2023 Page 26 of 43
the RC governing import of RTT samples, extracted in para 2
supra, required the details of the manufacturer and supplier to
be entered on the RTT Permit, which was also not done.
(iii) CCPL had sought to contend, before the RC, that the
RTT Sample had been manufactured by Jiangsu and exported to
India by Fertiagro under an Exclusive Service Agreement
30
dated 8 December 2010, executed between them. Given the fact
that, even as per the respondents’ case, Jiangsu was granted a
license for provisional manufacture of HSMT only in 2011, it
was obvious that no ESA could have been executed in 2010 for
sale, overseas, of the product of Jiangsu through Fertiagro.
(iv) Moreover, the Brief Note which was filed by the UOI
clarified that, in the application submitted by it for obtaining the
RTT Permit, CCPL had declared the supplier, as well as the
manufacturer, of the HSM 98%, as Fertiagro, Singapore.
(v) The documents on record revealed that Jiangsu had been
granted registration, in December 2013, for manufacture of
95% HSM, not 98% and that, in fact, registration for
manufacture of HSM 98% was granted only on 11 October
2018. The Registration Data relating to the registration granted
to Jiangsu in December 2013, as contained on the website of
the ICAMA, read as under:
Registered info
Registered number: LS20110312 First Dec Period: Dec 5,
30
"ES" hereinafter
LPA 215/2023 Page 27 of 43
Prove: 5,
2013
2014
ProductName: Halosulfuron-
methyl 95%
Toxicity: L
Formulation:
TC
Manufacturer: JIANGSU AGROCHEM
LABORATORY CO.LTD.
Country:
Remarks:
ActiveIngredient
Active Ingredient Content
Halosulfuron-methyl 95%
The learned Single Judge has, in para 22 of the impugned
judgement, clearly erred in holding that temporary registration,
for manufacture of HSMT 98% w/w, had been granted to CCPL
in 2011 vide Registration No. LS 20110312 and that permanent
registration was granted in 2013 vide Registration No. PD
20132005. In fact, Registration No. LS 20110312 was granted
on 5 December 2013 for manufacture of HSM 95%, not 98%,
and it was only with effect from 11 October 2018 that
registration had been granted to Jiangsu, vide Registration No.
PD 20132005, for manufacture of HSM 98%.
(vi) The Section 10 petition referred by appellant had been
rejected without any reasons.
(vii) Though the learned Single Judge has, in the impugned
judgment, observed that the record disclosed that Jiangsu was
manufacturing HSMT 98% in 2011, no such record was
forthcoming. In fact, this observation is contrary to the actual
record. In the process, the learned Single Judge ignored the data
relating to the registration is granted to Jiangsu for manufacture
LPA 215/2023 Page 28 of 43
of HSM and HSMT, as contained on the website of the
ICAMA, which was the registering authority.
(viii) Reliance on the decision taken in the 369
th
Meeting of the
RC held on 4 October 2016, vide Agenda Item No. 2.2, was
misplaced. The decision read thus:
“The committee further decided that no application with the
data generated using unauthorised sample (without
obtaining RTT permit) shall be accepted/processed on or
after the 1/01/2017. It was also decided that if any studies
of any product under any category is undergoing with such
samples, the same may be intimated to the APPA &
Secretary (CIB&RC) by 30/11/2016 through email at
cibsecy@nic.in. A Public Notice to this effect was also
issued.”
This decision referred to an unauthorised sample as one which
was without obtaining RTT permit. CCPL had, however,
obtained an RTT permit on 30 March 2011. The amnesty
granted in cases of studies of products under any category
undergone with such samples would not be available to CCPL,
as the manufacturer of the RTT Sample was declared as
Fertiagro, whereas the manufacture of the HSMT which was
sought to be imported under Section 9 was declared as Jiangsu.
(ix) On the aspect of locus standi¸ the Appellant relies on the
judgement of the Supreme Court in Jayaraj v. Commissioner
of Excise
31
.
II. Submissions of Mr. Arvind Nigam on behalf of CCPL
31
(2000) 7 SCC 552
LPA 215/2023 Page 29 of 43
28. Arguing for CCPL per contra, Mr. Nigam submits as under:
(i) The appellant had no locus standi to file the
appeal/revision application under Sections 10 and 11 of the Act.
(ii) The RC had evaluated the samples submitted by CCPL
on all parameters before granting Section 9(3) permission to
CCPL to import HSMT 98% w/w.
(iii) CCPL had, in 2011, procured the RTT sample from
Fertiagro. It was only after generating data and conducting all
tests and trials on the sample, which was confirming to 98%
purity, that CCPL submitted its application/dossier, along with
Form 1 on 11 April 2016, for grant of Section 9(3) registration.
On clarification being sought by the RC with respect to the
difference in the source of the HSM, as declared in the RTT
Permit and in the Section 9(3) application, CCPL had clarified,
vide letter dated 2 November 2016, that the sample which had
been imported by it under the RTT permit was in fact
manufactured by Jiangsu, though it was supplied by Fertiagro.
Further explanation and clarifications were provided by CCPL
before the RC at its 430
th
meeting held on 23 July 2021 and it
was only after consideration of the said explanation, and all
relevant facts and circumstances, that the RC granted
registration to CCPL to import HSMT 98% from Fertiagro,
manufactured by Jiangsu.
LPA 215/2023 Page 30 of 43
(iv) Jiangsu was, in fact, the authorised manufacturer of
HSMT in China since 2011. It had been granted temporary
registration to manufacture HSMT from the ICAMA in 2011,
and granted permanent registration in 2013. On 8 December
2010, the ESA had been executed between Jiangsu and
Fertiagro, under which Fertiagro was contracted to sell the
products of Jiangsu.
(v) A reading of the temporary registration No. LS 20110312
revealed that 95% was specified as a minimum. Tests and trials,
conducted on the HSMT revealed that it was having purity of
98%. The CCPL also had the products tested in the Central
Insecticide Laboratory, which disclosed that the purity of the
RTT sample was 98%.
In such circumstances, Mr. Nigam submits that the learned Single
Judge was justified in his decision not to interfere with the exercise of
subjective satisfaction by the RC.
E. Analysis
29. The balance, in such cases, has to be maintained between
restraint against interference with bona fide exercise, by the
competent executive authority, of discretion lawfully conferred by the
law on such authority, and ensuring that the mandate of the statute is
complied with.
LPA 215/2023 Page 31 of 43
30. From the times of Taylor v. Taylor
32
, through the judgment of
the Privy Council in Nazir Ahmed v. King Emperor
33
, through a host
of judgments of Supreme Court till as late as Mandeep Singh v. State
of Punjab
34
, the settled legal position is that, where the law requires a
particular act to be done in a particular manner, that act must be done
in that manner or not done at all, all other methods of doing the act
being necessarily forbidden. If, therefore, the manner in which
registration was granted to CCPL, to import HSMT 98% w/w,
following the decision taken in the 430
th
meeting of the RC held on 23
July 2021, infracts any mandate of the law, the decision would
become illegal, applying the Taylor v. Taylor principle. If, however,
no mandate of the law was breached while granting the registration,
then the Court would ordinarily defer to the exercise of discretion by
the executive authority, unless the exercise is found to be mala fide or
manifestly arbitrary.
31. Inasmuch as the registration was granted under Section 9(3) of
the Act, it is necessary to carefully read and understand Section 9(3).
Section 9(3) requires the RC to carry out “such enquiry as it deems
fit” and to satisfy itself “that the insecticide to which the application
relates conforms to the claims made by the importer or the
manufacturer as regards the efficacy of the insecticide and its safety to
human beings and animals”. Once the RC satisfies itself on these
aspects, registration may be granted, as sought by the applicant.
32
LR 1 Ch 426
33
AIR 1936 PC 253
34
2025 SCC OnLine SC 1420
LPA 215/2023 Page 32 of 43
32. The second proviso to Section 9(3) empowers the RC to deny
registration in a case where the applicant undertakes to put, in place,
precautions to ensure safety of the insecticide to human beings and
animals. However, the present case does not involve the application of
the said proviso.
33. Section 9(3) does not set out any empirical basis on which the
RC is to proceed while arriving at the requisite satisfaction regarding
safety and efficacy of the insecticide of which import, or indigenous
manufacture, is proposed. No guidelines can be gleaned from the said
provision. Section 5(5) of the Act, however, empowers the RC to
regulate its own procedure and the conduct of business to be
transacted by it. Section 36 of the Act empowers the Central
Government to make rules for the purposes of giving effect to the
provisions of the Act. In exercise of the powers conferred by the said
Section, the Central Government notified the Insecticides Rules in
1971. Rule 4 of the Insecticides Rules, in clause (b), empowers the
RC to carry out incidental or consequential matters necessary for
carrying out the functions assigned to it under the Act or the
Insecticides Rules. In exercise of the powers conferred by Section 5 of
the Act and Rule 4 of the Rules, the RC, from time to time, issues
Guidelines setting standards for regulating registration of insecticide
for export of indigenous manufacture, among other things.
34. Ms. Ramamoorthy laid emphasis on the decision of the RC,
taken in its 369
th
meeting held on 4 October 2016, not to accept or
process any unauthorised sample and, in the event of any studies of
LPA 215/2023 Page 33 of 43
any product under any category being still undergone in respect of
such sample, the requirement of intimation to the APPA and the
Secretary (CIB & RC). The words “unauthorised sample” has been
clarified in the decision taken on Agenda Item 2.2 by the RC in its
369
th
Meeting as a sample which was without obtaining RTT permit.
35. Though CCPL had applied under Section 9(3) for permission to
import HSMT 98% w/w and indigenously manufacture HSM 75%
WG on 11 April 2016, prior to the decision taken by the RC in its
369
th
Meeting which took place only on 4 October 2016, the addition
may still apply to CCPL’s application, as it referred not merely to
“acceptance” of the application, but also to “processing” of the
application. Inasmuch as the protocol represented a system put in
place in order to ensure that efficacy and safety of the pesticide, it has
to be strictly enforced, especially as the decision itself is not under
challenge before us.
36. Even so read, the entitlement of CCPL to registration under
Section 9(3), as applied on 11 April 2016, may not be seriously
affected by the stipulation. This is because the proscription, envisaged
in the said decision, was against acceptance or processing of an
application with data generated using an unauthorised sample, with
the words “unauthorised sample” being clarified as a sample which
was without obtaining RTT permit. There is no dispute that the data
which was enclosed by CCPL, while applying under Section 9(3), was
generated using the sample imported under the RTT permit dated 30
March 2011, issued by the RC itself. It cannot, therefore, be alleged
LPA 215/2023 Page 34 of 43
that the Section 9(3) application was accompanied by data which was
generated using an unauthorised sample.
37. The grant of registration to CCPL under Section 9(3) of the Act
cannot, therefore, be said to infract the decision taken by the RC in its
369
th
meeting, in Agenda Item 2.2.
38. Our attention has not been invited to any specific Guideline
issued by the RC, or other binding statutory or executive instrument,
which required an applicant under Section 9(3) to, prior to the
application, import a sample under an RTT permit, generate data and
use the said data as the basis for its subsequent Section 9(3)
application.
39. Ms. Ramamoorthy placed reliance, in this context, on the
“Guidelines for Import of Sample Quantity of Pesticides for Research,
And Trial (RTT) Purposes” issued by the RC consequent to the
decisions taken in its 148
th
, 245
th
and 329
th
meeting, reproduced in
para 2 supra. The reliance, to our mind, is misplaced. The said
Guidelines merely regulate import of sample quantities of pesticides
for RTT purposes. They cannot be read as enforcing a mandate to the
effect that an application under Section 9(3) must necessarily be
preceded by RTT’s testing of a sample and generation of data
therefrom.
40. This aspect may not, however, be of much significance in the
present case, as the fact of the matter is that CCPL in fact relied on the
data generated using the HSMT sample imported under the RTT
LPA 215/2023 Page 35 of 43
permit dated 30 March 2011. It was for this reason that, in the 429
th
meeting, the RC noted that there was a discrepancy in the source of
procurement of the HSMT as reflected in the RTT Permit and in the
Section 9(3) application submitted by CCPL. CCPL was, therefore,
directed to explain this discrepancy in the 430
th
meeting. CCPL claims
to have done so. Mr. Nigam’s contention is that the minutes of the
438
th
RC Meeting itself reflect that the various aspects pointed out by
CCPL were holistically considered by the RC, and an informed
decision taken to grant registration under Section 9(3), as was sought
by CCPL. This decision, according to Mr. Nigam, is not one which
invites interference by this Court under Article 226 of the Constitution
of India.
41. It is necessary, therefore, to examine the reliability of the
explanation proffered by CPL for the discrepancy of the HSMT, as
reflected on the RTT Permit and in the Section 9(3) application.
42. When we do so, we find ourselves unable to agree with the
learned Single Judge that the discrepancy stood satisfactorily
explained by CCPL and that, therefore, the Section 9(3) registration
had been lawfully granted to it.
43. It is worthwhile to reiterate, here, that grant of registration
under Section 9(3) has statutorily to be preceded by the arrival, by the
RC, of subjective satisfaction regarding the efficacy and safety of the
insecticide for which the application was made. In the case of CCPL,
the data produced by CCPL, as evidence of such safety and efficacy,
LPA 215/2023 Page 36 of 43
was the data generated by trial and testing on the sample imported
under the RTT permit. If the sample imported under the RTT permit
could not be equated with the insecticide of which import and
indigenous manufacture was being sought, it would become a case of
no evidence of safety and efficacy of the insecticide and, consequently,
of manifestly illegal grant of registration under Section 9(3).
44. The issue of whether the HSMT, of which the sample was
imported by CCPL under the RTT Permit, was the same as the
HSMT, for the import of which the Section 9(3) application had been
made by CCPL, therefore, acquires primordial significance.
45. Though the RC, in its 430
th
meeting, expressed satisfaction in
that regard, we are unable to agree that, before arriving at such
satisfaction, the discretion which vested in the RC was legally and
properly exercised.
46. Before elucidating why we so feel, we may dispense with the
submission of Ms. Ramamoorthy that the very requisitioning of an
affidavit, from CCPL, in the 431
st
meeting, was an indicator of the
fact that, prior thereto, the RC was not possessed of the requisite
satisfaction regarding the safety and efficacy of the HSMT, for the
import of which the Section 9(3) application had been filed by CCPL.
The mere requisitioning of an affidavit cannot, to our mind, operate as
conclusive evidence of the absence of any satisfaction having been
arrived at, prior thereto, by the RC. Affidavits, on many occasions, are
sought merely ex abundanti cautela. The calling for an affidavit
would bind the deponent down to the assertions in the affidavit, which
LPA 215/2023 Page 37 of 43
would confer additional sanctity thereto. The mere fact that, in its
431
st
meeting, the RC required CCPL to file an affidavit in the terms
stipulated in the said Meeting cannot, therefore, be of any substantial
significance.
47. At the same time, there are numerous infirmities which plague
the submission of CCPL that the sample of HSMT, which was
imported by CCPL under the RTT Permit granted to it on 30 March
2011, was also manufactured by Jiangsu.
48. In the first place, there is nothing to indicate that, in 2011,
Jiangsu had a registration, by the ICAMA, authorising it to
manufacture HSMT. No document to that effect, has been placed on
record, except the self-serving letter dated 10 August 2021, by
Jiangsu. The only two registrations granted to Jiangsu, which are
forthcoming on the record, are the registrations dated 5 December
2013 and 11 October 2018. The registration dated 5 December 2013 is
for manufacture of 95% HSMT. Though Mr. Nigam sought to contend
that 95% was stipulated as a minimum, there is nothing in the
registration certificate itself, as available on the website of the
ICAMA, to so indicate. A registration which has been granted to
manufacture HSMT 95% w/w cannot, quite obviously, be equated
with a registration which permits the manufacture of HSMT 98%
w/w. The registration of 11 October 2018 was much after the
application dated 11 April 2016 submitted by CCPL under Section
9(3) of the Act. The declaration, by CCPL, in its Section 9(3)
application that, on the date when the application was filed, Jiangsu
was authorised to manufacture HSMT 98% w/w was, therefore, not
LPA 215/2023 Page 38 of 43
supported by any material whatsoever. In fact, the material on record
would seem to indicate that Jiangsu did not hold any registration, as
on the date of filing of the application by CCPL under Section 9(3),
under which it could manufacture HSMT 98% w/w.
49. Even more significantly, in its application for grant of the RTT
Permit, CCPL declared the manufacture of the HSMT sample, as well
as the supplier of the sample, to be Fertiagro. As has been pointed out
by Ms. Ramamoorthy, it was necessary, in the event of the
manufacturer and supplier being two different entities, that the
application should specifically so state. The declaration, in the
application submitted by CCPL for obtaining the RTT Permit, of
Fertiagro as the manufacturer as well as the supplier, of the HSMT
sample, is irreconcilable with CCPL’s later assertion that the
manufacturer of the HSMT sample imported under the RTT Permit
was in fact Jiangsu, and that the supply had been effected through
Fertiagro.
50. In order to substantiate its stand that the HSMT sample which
had been imported under the RTT Permit was manufactured by
Jiangsu and supplied through Fertiagro, though the fact that the
sample had been manufactured by Jiangsu was not reflected either in
the application for grant of the RTT Permit or around the face of the
RTT Permit itself, Mr. Nigam placed reliance on the purported ESA
dated 8 December 2010. Unfortunately, the credibility of the ESA,
too, appears doubtful. The opening recital in the said ESA asserted
that Jiangsu was manufacturing HSMT 98%, in respect of which the
LPA 215/2023 Page 39 of 43
ESA had been executed. Ms. Ramamoorthy points out that this recital
is clearly incorrect as, even as per the respondents’ own showing,
Jiangsu was granted provisional registration to manufacture HSMT
98% only in 2011 (though no document evidencing such grant of
registration is on record). There is no explanation, from CCPL, as to
how Jiangsu could claim to have been manufacturing HSMT 98% on
8 December 2010, when the ESA was purportedly executed, when it
was granted provisional registration to manufacture HSMT 98%, by
the ICAMA only in 2011. This throws serious doubt on the credibility
of the ESA dated 8 December 2010.
51. Besides, if the RTT Sample had in fact been manufactured by
Jiangsu, there is no reason why this fact was not reflected either in the
application submitted by CCPL for grant of RTT permit, or on the
face of the RTT permit itself.
52. It is a matter of further concern that, in the Section 9(3)
application, not only the manufacturer, but also the supplier, of the
HSMT, were different from those named in the RTT permit. Not only
was the manufacturer Jiangsu, whereas Jiangsu was not reflected as
the manufacturer in the RTT permit, but the supplier was also no
longer Fertiagro but Hebei.
53. In this context, the presentation made by CCPL before the RC
in its 430
th
Meeting, and the manner in which the presentation was
addressed, makes for interesting reading. In the presentation, it is
stated that
LPA 215/2023 Page 40 of 43
(i) CCPL had procured the RTT permit for import of HSMT
from Fertiagro and had imported the HSMT as permitted by the
RTT Permit and generated data from the said imported sample,
(ii) the said sample was actually manufactured by Jiangsu
with whom Fertiagro had an ESA,
(iii) all required data in each discipline had been submitted by
CCPL,
(iv) an appeal had been filed by CCPL before the Appellate
Authority, which had noted that all scientific facts and complete
data had been given, while allowing the appeal on 2 December
2020,
(v) CCPL had submitted a letter to the Secretary CIB&RC
on 3 November 2016, informing the reason for the change in
the name of the source input and
(vi) CCPL had submitted a dossier, with a revised Form 1,
dated 11 April 2016, indicating the original manufacturer to be
Jiangsu.
The reference is, therefore, clearly only to facts such as an appeal filed
before the appellate order, to, various communications, most of which
were self-serving in nature, and other such data, with no reference to
any cogent material on the basis of which it could be said that the
RTT Sample had been manufactured by Jiangsu.
LPA 215/2023 Page 41 of 43
54. The RC, too, merely states that it “deliberated the agenda” and,
after considering points 5, 6 and 7, found that the case qualified for
registration under Section 9(3). We may note, here, that, though the
minutes refer to consideration of points 5, 6 and 7 of the 369
th
RC
Meeting, the minutes of the 369
th
RC Meeting do not, in fact, extend
till points 5, 6 and 7, as it is concluding at Point 3.1. The reference to
“points 5, 6 and 7” appear to be a reference to the immediately
preceding points 5, 6 and 7 of the presentation made by CCPL before
the RC in the 430
th
meeting, as itemised in Agenda Item 2.1.
55. Besides the fact that, without any further reasoning or
ratiocination, the RC merely proceeds to hold that it “found that this
case qualified for registration u/s 9(3)”, we are unable to comprehend
how such a conclusion could have been arrived at, from points 5, 6
and 7 of the presentation made by CCPL. Point 5 referred to Agenda
Item 2.2 of the minutes of the 369
th
Meeting of the RC dated 4
October 2016. We have already dealt with the said Agenda Item and
stated why, according to us, it is of no serious significance. Point 6
merely states the fact of a letter dated 3 November 2016 having been
submitted by CCPL to the Secretary CIB & RC and point 7 refers to
the submission, by CCPL, of a dossier with a revised Form 1 to the
CIB & RC Secretariat. None of these “Points”, therefore, provides
any explanation for the difference in the source of origin of
manufacture of the HSMT, has declared in the RTT Permit, and as
declared in the Section 9(3) application.
LPA 215/2023 Page 42 of 43
56. The inevitable conclusion is, therefore, that CCPL had not
provided the requisite data as could satisfy the RC that the sample
imported under the RTT Permit was from the same source as the
HSMT which CCPL desire to import, and for which it had applied for
registration under Section 9(3).
57. We are convinced that, in such circumstances, the RC was not
justified, in its 430
th
meeting, in granting Section 9(3) registration to
CCPL, as sought by it.
58. Inasmuch as satisfaction regarding the insecticide, for which the
application was made under Section 9(3), being safe and efficiacious,
is a sine qua non for grant of registration under the said provision, and
as we are not satisfied that CCPL had provided the requisite data as
could enable the RC to dispassionately and subjectively satisfy itself
on these aspects, we have no option but to set aside the grant, by the
RC, of registration to CCPL under Section 9(3) of the Act, pursuant to
the decision taken in the 430
th
meeting on 23 July 2021.
F. Conclusion
59. Resultantly, the registration granted to CCPL under Section
9(3), for import of HSMT 98% w/w and indigenous manufacture of
HSMT 75% WG, consequent to the decision taken in the 430
th
meeting of the RC conducted on 23 July 2021, as amended in the 431
st
meeting held on 27 August 2021, is quashed and set aside.
LPA 215/2023 Page 43 of 43
60. The impugned judgment of the learned Single Judge is also,
therefore, quashed and set aside.
61. The appeal stands allowed accordingly with no orders as to
costs.
C. HARI SHANKAR, J.
OM PRAKASH SHUKLA, J.
MAY 29 2026
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