IN THE HIGH COURT OF JHARKHAND AT RANCHI
SANJAY KUMAR DWIVEDI, J.
Krishna Nand Shastri @ K.N. Shastri – Petitioner
Versus
The State of Jharkhand – Respondent
Cr. M.P. No. 1525 of 2014
Decided On : 03-05-2023
| Table of Content |
|---|
| 1. details of the criminal proceedings against the petitioners. (Para 1 , 2 , 3) |
| 2. arguments regarding the lack of allegations against the petitioners. (Para 4 , 5 , 6) |
| 3. court's analysis of the legal requirements under section 202 cr.p.c. (Para 7 , 8 , 9) |
| 4. conclusion quashing the criminal proceedings. (Para 10 , 11 , 12) |
JUDGMENT :
SANJAY KUMAR DWIVEDI, J.
1. Heard Mr. Pandey Neeraj Rai, the learned counsel appearing on behalf of the petitioners and Ms. Kumari Rashmi, the learned counsel appearing on behalf of the respondent-State.
2. This petition has been filed for quashing of the entire criminal proceeding in connection with G.O.C.R. No. 61 of 2013, T.R. No. 879 of 2014 including order taking cognizance dated 15.07.2013 pending in the court of learned Chief Judicial Magistrate, Deoghar.
3. The complaint case has been lodged alleging therein, in nutshell, that On 02.03.2011 the then Inspector of Drugs inspected premises of M/s. Bajpai Medicals, Deoghar and the Inspector issued Form-16 on Ciproplus BWS, 100 mg manufactured by M/s. Intercorp Biotech, New Delhi and as per the composition mentioned on the label ciprofloxacin hydrochloride-100 mg is present in 1 gm of the product, which implies that the product is a drug but no drug manufacturing license No. is mentioned on the label and the product is sold as ‘nutritional supplement’. The said company was informed regarding the seizure and it was asked to produce the constitution details of the firm. The manufacturer requested for 15 days’ time. After receipt of the judgment of Hon’ble High Court, the Drug Inspector sought approval for prosecution from the Director in Chief (Drugs) to prosecute the manufacturer company under section 27(b) and (d) for violation of section 18(a) and (c) of the Drugs and Cosmetics Act, 1940 and in turn approval has been granted. The special leave petition preferred by the manufacturer before the Hon’ble Supreme Court was dismissed. Ciprofloxacin Hydrochloride is a potent antibacterial agent which is categorized under schedule-H of the Drugs and Cosmetics Rules, 1945. The manufacturer by claiming ciprofloxacin hydrochloride as a nutritional supplement has tried to misguide and hamper the instigation process. The manufacturer distributed and sold the drug without obtaining the drug manufacturing license which violates section 18(c) and is punishable under section 27(b). Hence this case.
4. The learned counsel for the petitioners submits that the complaint case was lodged on 12.7.2013 and on the same day the learned court has taken cognizance on 15.7.2023. He submits that however it appears that summons have been issued on same day. He submits that the petitioners are the Directors of the company in question. He submits that in the entire complaint there is no allegation that these petitioners are looking into the day to day affairs of the company and to buttress his argument he has relied in the case of State (NCT of Delhi) v. Rajeev Khurana , 2010 (11) SCC 469 , paragraph Nos.17 of the said judgment is quoted below:
5. The learned counsel for the petitioners submits that the petitioners were stationed at Delhi and it is also admitted in the complaint and the learned court without following the mandatory provision under section 202 Cr.P.C. has taken cognizance which is against the mandate of law.
6. On the other hand, Ms.
State (NCT of Delhi) v. Rajeev Khurana
Udai Shankar Awasthi v. State of U.P. and Another
M/s. Maithon Power Limited and Others v. State of Jharkhand and Others
The central legal point established in the judgment is the exemption of the drugs manufactured by the petitioner from the provisions of Chapter IV of the Drugs and Cosmetics Act, 1940 under Schedule ....
Manufacturing bleaching powder not intended for medicinal use is exempt from licensing under the Drugs and Cosmetics Act, 1940.
Distributors of drugs are not liable for quality issues if they prove acquisition from a licensed manufacturer and proper storage, as per Section 19(3) of the Drugs and Cosmetics Act.
Vicarious liability of directors in criminal cases and the requirement for proper recording of materials for taking cognizance under the Drugs and Cosmetics Act.
Non-compliance with inspection procedures under the Drugs and Cosmetics Act, 1940 is not fatal for prosecution in cases involving allegations of spurious drugs.
Right of appellant to have sample analysed in Central Laboratory is a valuable right.
Login now and unlock free premium legal research
Login to SupremeToday AI and access free legal analysis, AI highlights, and smart tools.
Login
now!
India’s Legal research and Law Firm App, Download now!
Copyright © 2023 Vikas Info Solution Pvt Ltd. All Rights Reserved.