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READ ONCE | POWER CORRUPTS : ABSOLUTE POWER CORRUPTS ABSOLUTELY
DRUGS CONSULTATIVE COMMITTEE (DCC)
1. In the year 1993 guidelines in respect of NSQ drugs were circulated amongst all State Drug Controllers.
2. NSQ drugs were divided into ‘Major’ and ‘Minor’ defects and guidelines were issued for taking appropriate actions
3. Investigation is the important part of those guidelines before proposing any action whether administrative or legal.
4. Prosecution was stated to be last resort where all other remedial measures had failed.
GUIDELINES FOR TAKING ACTION ON SAMPLES OF DRUGS DECLARED SPURIOUS OR NOT OF STANDARD QUALITY IN THE LIGHT OF ENHANCED PENALTIES UNDER THE DRUGS AND COSMETICS (AMENDMENT) ACT, 2008 Effective from 10.8.2009.
Legal/administrative actions as required under the said Act and Rules for the violation of the provisions of the Act are taken by the State Licensing Authorities. The actions are normally initiated on the basis of test reports of Government analysts declaring the drug samples as not of standard quality. The major categorization of not of standard quality reports could be as under:-
Category A (Spurious and Adulterated Drugs
Category B (Grossly sub-standard drugs)
Category C (Minor defects)
In the case of drugs manufactured by a licensed manufacturer under a valid manufacturing licence has been found grossly sub-standard, the matter may be investigated at the manufacturer’s end, and where criminal intent or gross negligence has been established and if the merits of the case so demand, and where it is felt that administrative measures would not be sufficient to meet the ends of justice, the re-course to prosecution should be resorted to,
In the case of drugs manufactured by a licensed manufacturer under a valid manufacturing licence and found grossly sub-standard and where criminal intent or gross negligence is not established, weapon of prosecution should be used judiciously, where it is felt that administrative measures like suspension or cancellation of licenses or compounding of offences would not meet the ends of justice.
In the case of not of standard quality reports because of minor defects arising out of variations from the prescribed standards or contraventions of other provisions of chapter IV of the Act, administrative measures including suspension/cancellation or compounding of offences may be resorted to. Prosecution may only be launched where it is justifiably felt that above measures would not meet the ends of justice.
The State Drug Control Departments shall constitute screening committees comprising of at least three senior officers not below the level of Assistant Drugs Controllers or equivalent to examine the investigation reports of the cases where prosecutions are proposed to be launched. The committee may submit written opinion on the investigation reports regarding their feasibility of taking legal action.
The criminal intent or gross negligence should be taken into consideration while recommending actions like prosecution etc. Care should be taken that charges framed are not based on inappropriate provisions which may be difficult to prove in the court of law in the absence of proper justification or evidence. Cases of failing in assay, brand name disputes and non-renewal of manufacturing licence in time should be examined on their merits before recommending prosecution in such cases.
Prosecutions by the Inspectors shall be launched on the basis of written permissions of the controlling authority and this authority in turn shall consider the opinion of the screening committee while taking final decision in the matter.
Prosecutions under section 18(a)(i) r/w sec. 27(d), in case drug is declared NSQ, barring some exceptions, are being launched against firms/companies, mostly SMEs’, across the country, no body in the profession is objecting and raising the voice, judiciary is also taking cognizance of alleged offence and criminal matters attracting vicarious liability are dragging in various Courts not only for years but for decades causing undue hardship to so called accused persons in addition to mental agony, torture, humiliation and financial burden.
Well if reporting of a drug as NSQ is the basis for launching the prosecution then nearly 10000 (Ten thousand) samples reported NSQ annually must result in prosecution in each and every case. But it does not happen so and the system of ‘pick and choose’ is being adopted depending on the ‘deal’, size and category of the company and its influence on the FDA, superior officials and political leadership.
The author is of the firm view that simply if a drug is declared as Not of Standard Quality (NSQ) and even if the test report either in form 13 or in form 2 is accepted as it is, there is no contravention of sec. 18(a) (i) and nor legislator has prescribed any punishment u/s 27(d) under such circumstances UNLESS:
It is established, on real investigation
1. That while the drug was manufactured and released for sale/distribution, it was not properly manufactured/tested for some or the other reason, either partially or wholly. OR
2. That the drug is NSQ and falls within the ambit of sec. 27(a) of the ‘Act’. OR
3. That the drug was being sold / distributed even after receipt of adverse test report.
There is no provision in the ‘Act’ for punishment under sub-sections (a), (b), (c) and (d) of sec. 27 if the drug is allegedly declared as NSQ and if findings in the investigation, in above respect, is negative.
Hon’ble Supreme Court while dealing with a case on limitation (State of Rajasthan Vs Sanjay Kumar and Others Drug Cases 1998, SC, 7), under Para 9 have observed as under:
“On the date of collection of samples from respondent no. 16, on February 29, 1988, it could not have been said that any offence was committed as selling of drugs per se is no offence and the quality of drugs was not known to the Drugs Inspector, the complainant on that date. It is only, when the report of the Government Analyst was received, that it came to light that the provisions of the Act are violated and offence is committed.”
Thus it is only on receipt of the adverse test report by the Drugs Inspector, subject to investigation and scrutiny thereof technically, it could be attributed that the offence, if any, is committed. The responsibility could be fastened on person(s) after detailed investigation.
While disposing of bundle of Criminal applications on the issue of tenability of Regular Criminal cases, Hon’ble Bombay High Court, Bench at Nagpur made following observations:
“Looking to the scenario discussed by me above, I conclude that the Food and Drugs Department and its officers from the cadre of Food Inspectors to Joint Commissioner do not have any legal knowledge, legal skill and seriousness with which the provisions of these Acts concerning human health is required. They are casual, callous and hardly concerned. Relevant and concerned provisions/amended provisions of Code of Criminal Procedure are not even known to them to make use thereof.
They are making cases only to show that cases are being prepared and instituted in Courts and finally tell the people that Courts have discharged or acquitted the accused persons and thus save their skin. In my opinion, Government is simply wasting money on Food and Drugs Department and serious view for revamping this department will have to be taken by the Government with strict “accountability” to be fixed for each and every officer”. (Bombay High Court, Nagpur Bench, Cr.Appl. Nos. 3439 of 2006 with Cr. Appl. Nos. 3440 of 2006, 3442 of 2006, 3444 of 2006, 3441 of 2006, 3445 of 2006, 1290 of 2008 and 3443 of 2006)
In the same matter Hon’ble Court, was pleased to direct as below, under Para 23, to the Secretary, Food and Drug Department:
“I have already pointed out in details in para 7,8,9,19,20 & 21 the acts of omissions and commissions on the part of the officers of the department and I clearly find that the officers of the Food and Drug Department in these cases who are public servants have disobeyed the law with intention to cause injury by their acts of omissions and commissions and thus they have committed offence punishable under section 166 of Indian Penal Code.
Since the offence is noncognizable, this Court directs the Secretary, Food and Drug Department, Government of Maharashtra, to identify the concerned officers responsible for the acts of omissions and commissions in all these cases and cause filing of private complaint for the offence punishable under section 166 of Indian Penal Code against them in the Court of law, and report compliance about filing thereof to this Court on or before 31.7.2010”.(www.indiankanoon.com)
A Firm/Company whose drug is alleged to have violated prohibitory provisions under section 18 (a) (i) is invariably sought to be punished under section 27 (d) of the ‘Act’.
Each and every licencee authorized to manufacture drugs for sale or distribution complies with mandatory provisions of Drugs and Cosmetics Rules 1945 (Rules) in as much as that every raw material is utilized in formulation only on its compliance with prescribed standards and the finished goods is released for sale /distribution only when the batch is reported as of standard quality conforming with prescribed standards.
Every licencee maintains proper record of raw material and finished goods as prescribed under ‘Rules’. The testing of raw material and finished goods is conducted either in in-house laboratory of the licencee or in an institution duly approved by the SLAs under the provisions of the ‘Rules’.
In-house testing unit of the licencee and the institution approved by SLAs are subjected to FDA inspections periodically for maintenance of Qualified Staff, Equipments, Instruments, and Methods of analysis adopted, Chemicals/Reagents, floor area etc.
Subsequently on reporting of a drug/batch NSQ by the GA the process begins. The so called ‘Investigation’ carried out by Drugs Inspector (DI) concerned before launching of prosecution in the Court of Law, is nothing but collection of record related to manufacture, testing, sale, constitution of the firm, names and residential addresses of technical staff responsible for the manufacture and testing of disputed drug, licence copies with renewal, if any.
For collection of these records, some State Authorities have adopted a practice (?) to visit the licencee, may be located in other States, with or without the local FDA Authorities. In the meanwhile the SLA in whose jurisdiction the licencee operates normally serves Show Cause Notice (SCN), to such licencee, under rule 85 of ‘Rules’.
Thereafter depending of whims of concerned DI and his superior Authorities, the private complaint (Prosecution) is launched in the Court of Law alleging contravention of sec. 18(a) (i) and seeking punishment u/s 27(d) of the ‘Act’. There is not a single known example in the country where the Court did not take cognizance of the matter applying judicial mind as has been observed by High Courts in number of judgments and dismissed the complaint ab-initio.
It is reiterated that solely on the basis of author’s interpretation of secs. 18(a) (i) and 27(d) that if a drug/batch is reported as NSQ and even if the said report is accepted as it is, and if the relevant batch of the drug is not sold by the licencee thereafter, there is no contravention of sec. 18(a)(i) and sec. 27(d) does not prescribe any punishment in such circumstances. This legal thought is being narrated in sequence as under:
a) The allegation that the accused have manufactured the drug/batch as NSQ and sold/distributed the same as such is unfounded, without any evidence to that effect. On the contrary the record related to manufacturing/testing may or may not be filed with the complaint goes to establish beyond any doubt that the drug/batch when was manufactured and released for sale/distribution, was of Standard Quality. There is practically no specific allegation that what material in those records would be treated as supportive to the allegation made in the complaint.
b) It is the test report issued by the GA opining that the drug/batch is NSQ at a subsequent date is the basis of presumption that the drug/batch must have been NSQ when manufactured and sold/distributed.
c) Hon’ble Supreme Court of India in the matter between State of Rajasthan Vs Sanjay Kumar and Ors, (DC 1998, SC, 7) in Para 9 observed as
“On the date of collection of samples from respondent no. 16, on Feb. 29, 1988, it could not have been said that any offence was committed as selling of drugs per se is no offence and the quality of drugs was not known to the Drugs Inspector, the complainant on that date. It is only when the report of the Government Analyst was received, it came to the light that the provisions of the Act are violated and offence is committed.”
d) Allegation of contravention of s.18 (a) (i) seeking punishment u/s 27(d) of the ‘Act’ could be possible only if:-
i) There is documentary evidence that at the time of release of drug/batch for sale/distribution and based on manufacturing and testing record the drug was in fact Not of Standard Quality (NSQ) at that itself.
There is not a single known example where allegation of violation of sec. 18(a) (i) is levied with aforesaid or any similar documentary evidence with the complaint or otherwise.
The Drugs Inspector and all other superior officials in the Regulatory in the Centre and States, baring exceptions, are claiming to be qualified and experienced in the profession and therefore, in appropriate cases investigation on above technical aspect is definitely expected. Such officials are not supposed to act as ‘Bada Babu’ and ‘Babu’.
ii) The manufacturer-licencee continues sale/distribution of disputed drug even after receipt of adverse test report. Almost in each and every case no unsold stock of the disputed drug is available with the manufacturer-licencee, at the time when such adverse test report is received by it, therefore, question of sale/distribution of disputed drug after receipt of adverse test report does not arise and any allegation to that effect is unlawful and unfounded.
On the contrary in 100% cases, the manufacturer-licencee, on being directed, as provided u/r 74(j), 78(i) by the State Licensing Authority, initiates effective steps to recall stocks of disputed drug/batch, as for as practical, from the market/institutions to whom the said drug was sold. The manufacturer-licencee is also required to intimate SLA of the quantity, if any, received back from the market and ensure its due destruction in presence of FDA official.
e) The object of sec. 18(a) (i) also aims at dealers/institutions etc. who if ignore the intimation about adverse test report received either from the DI or manufacturer-licencee and continue the sale/distribution etc. of the disputed drug/batch. In such circumstances and if due investigation is carried out only such dealers/institutions are liable to be prosecuted.
f) There is no provision in sec. 27 to punish any body even if a drug/batch is found NSQ, except as described above, and except as provided u/s 27 (a), if attracted, the relevant portion is abstracted here below:
“Solely on account of such drug being adulterated or spurious or not of standard quality, as the case may be”
Which means any drug if is likely to cause death or is likely to cause such harm on the body as would amount to grievous hurt within the meaning of sec. 320 of Indian Penal Code solely on account of such drug being not of standard quality, is punishable. Sub-sections (b) and (c) of sec. 27 are not relevant to this article.
Sub-section (d) of sec. 27 being residual section is invariably applied seeking punishment for violation of sec. 18(a) (i) particularly for drug reported NSQ. This section provides punishment for any drug, other than a drug refered to clause (a) or clause (b) or clause (c) in contravention of any other provision of this chapter or any rule made there under.
Now if we relook at sec. 18(a) (i) which is prohibitory provision and as demonstrated above, there is hardly any evidence in support of allegation that the drug/batch when manufactured and sold was NSQ at that stage only; seeking of punishment u/s 27(d) is absolutely irrelevant. In other words sec. 27(d) does not prescribe any punishment even if drug/batch is reported NSQ unless and until prohibitory provision of sec. 18(a) (i) is contravened.
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