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2024 Supreme(P&H) 45

IN THE HIGH COURT OF PUNJAB AND HARYANA AT CHANDIGARH
HARPREET SINGH BRAR, J.
Suresh Jindal and another – Appellants
Versus
State of Punjab - Respondent
CRR No.241 of 2024 (O&M)
Decided on : 06-02-2024

Advocates:
Advocate Appeared:
For the Appellant : Mr. Sapan Dhir

The evaluation at the stage of framing of charge is to test the existence of a prima facie case, and the court cannot delve into the probative value of the material on record.

Headnote:

Drugs and Cosmetics Act - Manufacturing of Hand Sanitizer - Sections 17A, 18(a)(i), 27(b)(i) & 27(c) - Act of 1940

Fact of the Case:

The petitioners, engaged in the manufacturing and sale of pharmaceutical products, were charged under Sections 17A, 18(a)(i), 27(b)(i) & 27(c) of the Drugs and Cosmetics Act, 1940 for the sale of a hand sanitizer declared as not of standard quality by the Government Analyst.

Finding of the Court:

The court found no force in the petitioners' arguments and upheld the framing of charges, citing the test of existence of a prima facie case at the stage of framing of charge.

Issues: The issues revolved around the compliance with storage conditions, testing procedures, and the evaluation of a prima facie case at the stage of framing of charges.

Ratio Decidendi: The court emphasized that at the stage of framing of charge, the evaluation is to test the existence of a prima facie case, and the court cannot delve into the probative value of the material on record.

Final Decision: The petition was dismissed, and the trial court was directed to proceed without being prejudiced by the observations of the High Court.

JUDGMENT :

HARPREET SINGH BRAR, J.

1. The present revision petition has been filed by the petitioners seeking quashing of the impugned order dated 06.11.2023 passed by the Judge, Special Court, Rupnagar vide which charges have been framed against the petitioners under Sections 17A, 18 (a) (i), 27 (b) (i) & 27 (c) of the Drugs and Cosmetics Act, 1940 (hereinafter referred to as the Act of 1940).

2. In brief, facts are that petitioner No.2 Firm namely Ms Cosway Pharmaceuticals is engaged in the business of manufacturing of all kinds of tablets, capsules, oral syrups, ointments and other pharmaceutical products at Plot No.11-C, Industrial Area, Tahliwal, Tehsil Haroli, District Una (HP) as well as in sale distribution of drugs specified in Schedule C & C (i) in Forms 25 & 28 under Licence No.N-MB15157 & N-MB15158 dated 03.03.2017 issued by the Assistant Drugs Controller-cum-Drugs Licensing Authority. Petitioner No.1 is one of the partners of the said firm. On 06.03.2020, petitioner No.2-Firm purchased raw material for manufacturing Cosway Hand Sanitizer from Ms Mahaveer Agencies, Nalagarh along with testing report analysis certificate dated 19.02.2020. On 16.03.2020, the abovesaid product was got approved from the Assistant Drugs Controller-cum-Drug Licensing Authority, District Kangra and after obtaining approval from the said authority, the said product ‘Cosway Hand Sanitizer (Safe & Clean) bearing Batch No.C-02, Mft. Date 42020, Exp. Date032022 was got tested from the Central Government approved laboratory as well as the in-house testing on 2425.04.2020, before releasing the same in the market. Copies of approval dated 16.03.2020 granted by the Licensing Authority and the Analysis Certificate dated 25.04.2020 are annexed with the present petition as Annexure P-3. Thereafter, after release of the product in the market, one of the retailers of petitioner No.2-Firm namely Ms Gupta Medical Agencies at Ropar purchased the same vide invoice No.040 dated 06.05.2020. On 08.05.2020, the Drug Inspector, Ropar inspected the premises of Ms Gupta Medical Agencies and obtained sample No.RPRTS202029 (four portions of 2x100 ml of Cosway Hand Sanitizer (Safe & Clean) (Isopropyl Alcohol, Carbopol, Carbopol, Triethanolamine, Glycerine & Chlorhexidine Digluconate Hand Sanitizer), Batch No.C-02, Mfg. Date0420, Exp. Date032022 from the said premises. The said sample was sent to Government Analyst, Punjab, Chandigarh for testing and analysis on 11.05.2020, who vide report dated 29.06.2020 declared the sample in question as not of standard quality. On receipt of aforesaid report, the Drug Inspector enquired about the source from where the product was purchased by Ms Gupta Medical Agency and ultimately, it came forth that the product in question was manufactured by the petitioner No.2-Firm. Thereafter, vide letter dated 01.09.2020, the Drug Inspector, while sending the analysis report dated 29.06.2020 to the petitioners, had sought response of petitioners with respect to the same and to adduce evidence in writing within 28 days of receipt of the letter. Vide letter dated 15.09.2020, petitioners replied that at the time of manufacturing, they had complied with all requirements as per the Act of 1940 and because they were not satisfied with the testing done, they requested for re-assessment of the sample as per the provisions of Section 25 (3) of the Act of 1940. However, despite specific request made by the petitioners for providing sample to them and without asking from them the working standard and method of analysis as per the guidelines of Central Drugs Standard Control Organization (CDSCO), the Drug Inspector sent the sample in question to the Central Drugs Laboratory, Calcutta on 11.01.2021, which gave report dated 04.08.2021 contrary to the earlier report dated 29.06.2020 given by Government Analyst, Punjab. Another sample from the same batch of the product was also sent to the Government Analyst, Chandigarh, who vide his report dated 05.09.2020, h

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