(1.) The applicant has been convicted under Section 18 (a) (i) and (ii) of the Drugs Act. A Municipal Medical Officer of Health took a sample; of a medicine called Gripex on 10-11-1955 from the shop of the applicant and sent it for analysis. The Government Analyst after analysis gave has report on the prescribed form that it was substandard but did not give the protocols of the test applied by him. The report was received in evidence against the applicant and on its basis he has been convicted. The Government analyst himself was not examined as a witness to prove the tests applied by him.
(2.) On the date on which the Municipal Medical Officer of Health took the sample, the Drugs Act of 1940 stood amended by the Act of 1955. Section 21 of the Act as it stands now empowers a State Government to appoint such persons, as it thinks fit "having the prescribed qualifications, to be Inspectors for the purposes of this Chapter within such local limits as it may assign to them respectively". Under Section 33 the Central Government has been empowered to make rules prescribing qualifications of Inspectors. In exercise of that power, in June, 1957, the Central Government made the Drugs Rules. Rule 49 prescribes the qualifications for an Inspector, it is subject to three provisos, the last one being that for the purposes of inspection of shops in any specified area any officer of the medical or public health department, who is a graduate in science, may be appointed an ex-officio Inspector. No appointment has" been made by the State of Uttar Pradesh after 1955. Prior to the amendment of the Act in 1955, the power to prescribe qualifications for an Inspector vested in the State Governments and in exercise of that power the State of Uttar Pradesh had made Rule 49 prescribing qualifications for an Inspector. Those qualifications were exactly the same as are mentioned in Rule 49 of the Drugs Rules made in 1957, with this difference that in the last proviso it was said that for the purposes of inspection of retail shops, any officer of the public health department, who was a graduate in science, could be appointed an ex-officio Inspector. Accordingly in 1954 the State Government had issued a notification appointing all officers of the public health department (they were all graduates in science) as ex-officio Inspectors for inspection of retail shops. No appointment of an Inspector has been done by the State Government subsequently. The Municipal Medical Officer of Health, who took the sample in the present case, is an officer of the public health department and graduate in science and was appointed an Inspector for inspection of retail shops within his district. It is not known whether the shop of the applicant is a retail shop or a wholesale shop; there is no evidence on the record. If it is a wholesale shop, the Municipal Medical Offfcier of Health was not empowered even to inspect it. Section 22 of the Act lays down that subject to any Rules made by the Central Government in this behalf, an Inspector may take samples of any drug, but if an Inspector is appointed for a purpose other than that of taking samples, he is not an Inspector within the meaning of this provision of Section 22. The word 'Inspector' occurring in the beginning of Section 22 means an 'Inspector' with reference to the particular power that is sought to be exercised; a person who is appointed an Inspector for the exercise of a particular power does not become an Inspector within the meaning of Section 22 for the exercise of any other power mentioned in Sub-section (1). Under Section 33 fn) the Central Government has the power of regulating the powers and duties of Inspectors and in exercise of this power it has made Rule 51 laying down that an Inspector authorised to inspect premises licensed for the sale of drugs must inspect all establishments licensed for the sale of drugs at least twice a year and procure and send for test or analysis, if necessary, samples of any drug, which he has reason to suspect is being sold or stocked or exhibited for sale in contravention of the provisions of the Act or Rules made thereunder, and to institute prosecutions in respect of breaches of the Act and the Rules made thereunder. The Municipal Medical Officer of Health having been appointed for inspection of retail shops may not be said to be an "Inspector authorised to inspect premises licensed for the sale of drugs"; a retail shop may not have been licensed at all. In the present case, the applicant has been found not to have a proper licence for the shop. Consequently, it can be said that an Inspector appointed for inspection of retail shops has not the powers conferred by Rule 51 and cannot procure and send for test or analysis samples of any drug. His power is confined to making an inspection of retail shops and the power to inspect does not include the power to procure and send samples for test or analysis. Had the Municipal Medical Officer of Health been appointed an Inspector for the purpose of inspecting premises licensed for the sale of drugs and had the applicant's premises been licensed for the sale of drugs, he could not only inspect them but also (under the authority of Rule 51) procure and send for test or analysis samples of any drug sold or stocked therein. That is not the case here and the Municipal Medical Officer of Health must be held to have had no power to procure and send for test or analysis the sample of Gripex. Sections 23, 24 and 25 would come into application only when a sample is taken by an Inspector under Section 22(1) (b). If it is taken by a person who is an Inspector! for a certain purpose but not for the purpose of taking a sample, Ss. 23, 24, 25 etc. will not apply and even if he gets the sample analysed by a Government Analyst and the Government Analyst sends his report signed by him, the report cannot be evidence of the facts stated therein. The Government Analyst may in that case be examined as a witness to prove his opinion by oral testimony but his report itself would not be evidence. Consequently, in the present case, the report of the Government Analyst could not be treated as evidence.
(3.) There is a serious defect in the report of the Government Analyst and it is that full protocols of the test are not supplied. The report is in the prescribed form but all the headings are not fully answered. One of the headings of the prescribed form is "Result of test or analysis with protocols of test applied". The report contains only the result of the test or analysis. When it does not state the protocols of the test applied, it cannot be said to be a report "in the prescribed form." The mere use of the prescribed form containing the headings will not make it a report "in the prescribed form" if all the headings are not duly filled in, If there is an omission to fill in a certain heading and the omission does not cause any prejudice, it may be held that the report is still in the prescribed form but the omission to state either the result of the test or the protocols of the test applied is a substantial omission which goes to the root of the existence of the report "with prescribed form". It is necessary for the accused to have full information about the protocols of the test applied so that he may be in a position to controvert the result by producing evidence, which power has been conferred upon ham by S, 25 (3). If he does not know the protocols of the test, he would not be in a position to adduce evidence! to controvert the report by showing that the test applied was not a conclusive test or was not a correct test. If the protocols of the test are not stated in the report, the report must be held to be not a report "in the prescribed form" within the meaning of Section 25 and cannot be treated as evidence of the facts stated therein. If the report cannot be treated as evidence, the Government Analyst must himself be examined as a witness to prove his opinion; otherwise the case will not be roved against the accused. Note to form No. 13, by which the form of report is prescribed, provides that no protocols of test applied are necessary in respect of patent and proprietary medicines which are registered at the Central Drugs Laboratory. There is no evidence on the record to show that Gripex is a patent or proprietary medicine registered at the Central Drugs Laboratory, and it cannot be assumed that no protocols of the test applied were necessary. If the Government Analyst refrained from supplying the protocols because of the registration, he should have referred to it in there-port or the prosecution should have produced evidence to prove that Gripes is a patent or proprietary medicine registered at the Central Drugs Laboratory. Had such evidence been produced, there would have been no defect in the report and it would have been treated as evidence under Section 25(3).