This document contains 20 multiple choice questions related to the registration of drugs and advertising of drugs in Pakistan. The questions cover topics such as the qualifications and roles of members of the registration board, procedures for registering and advertising drugs, pricing and promotional regulations. The document was submitted by Iqra Zaman Kayani to Dr. Zirwa as part of a 5th professional year class on forensic pharmacy.
This document contains 20 multiple choice questions related to the registration of drugs and advertising of drugs in Pakistan. The questions cover topics such as the qualifications and roles of members of the registration board, procedures for registering and advertising drugs, pricing and promotional regulations. The document was submitted by Iqra Zaman Kayani to Dr. Zirwa as part of a 5th professional year class on forensic pharmacy.
This document contains 20 multiple choice questions related to the registration of drugs and advertising of drugs in Pakistan. The questions cover topics such as the qualifications and roles of members of the registration board, procedures for registering and advertising drugs, pricing and promotional regulations. The document was submitted by Iqra Zaman Kayani to Dr. Zirwa as part of a 5th professional year class on forensic pharmacy.
This document contains 20 multiple choice questions related to the registration of drugs and advertising of drugs in Pakistan. The questions cover topics such as the qualifications and roles of members of the registration board, procedures for registering and advertising drugs, pricing and promotional regulations. The document was submitted by Iqra Zaman Kayani to Dr. Zirwa as part of a 5th professional year class on forensic pharmacy.
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MCQS
FORENSIC PHARMACY TOPIC: REGISTRATION OF DRUGS & ADVERTISING OF DRUGS SUBMITTED TO: DR. ZIRWA SUBMITTED BY: IQRA ZAMAN KAYANI CLASS: 5TH PROF YEAR
1. One expert having atleast _____ years
of experience in the field of veterinary medicine to be nominated by the federal government. a) 12 b) 16 c) 15 d) 10 2. One expert having atleast _____ years of experience in the field of pharmacology to be nominated by the federal government on te recommendations of the authority. a) 10 b) 15 c) 7 d) 6 3. One law expert to be nominated by the law, justice and human rights division who shall not be below _____ a) BPS-19 b) BPS-5 c) BPS-60 d) BPS-20 4. The deputy director general, registration, drug regulatory authority of Pakistan who shall be its _____ a) Dean b) Secretary c) Ex-officio secretary d) HOD 5. The registration board may refer any case for detailed examination to the _____ on the drugs evaluation constituted under section 10 of the act. a) Appellate board b) Committee of experts c) Deputy director d) Supreme court 6. The registration board may appoint a sub-committee consisting of atleast one clinical professor, one pharmacologist and _____ pharmacist to make a detailed examination of each case. a) 2 b) 1 c) 3 d) 5 7. The chairman himself or on the directions of the _____ of the drug regulatory authority of Pakistan, may call meeting of the board. a) Chief executive officer b) Director c) Supervisor d) Drug inspector 8. In the absence of chairman, the _____ may elect one of the members to preside over the meeting. a) Director b) Hod c) Board d) Drug inspector 9. The agenda for a meeting shall be circulated to the members atleast _____ days prior to the meeting a) 10 b) 7 c) 2 d) 15 10. In deciding applications for registration, first priority shall be given to the _____ units. a) Inspection units b) Registration board c) Appellate board d) Newly-licensed
11. A fee of rupees _____ shall be paid for
the duplicate copy of the certificate of registration if the original is defaced, damaged or lost. a) 50 b) 100 c) 200 d) 250 12. A certificate of registration of drug shall be issued in form _____ a) 2 b) 7 c) 10 d) 6 13. The indenter, importer or manufacturer’s authorized agent shall issue a ____ in Form 2-A for any drug indented or sold by him for the purpose of resale or distribution. a) Warranty b) Guarantee c) Record d) Payment 14. A record of quarterly production and disposal of adrug shal be maintained and supplied to the chairman of the registration board in Form _____ a) 8 b) 10 c) 7 d) 4 15. The manufacturer or, as the case may be, the indentor should follow the ethical criteria for medical drug promotion as given in _____ a) Record b) File c) Schedule F d) Schedule G 16. An application for advertisement of any drug, substance, remedy, treatment or offer of treatment for any disease shall be made in ____ a) Form 7 b) Form 8 c) Form 9 d) Form 10 17. An application under sub-rule (1-A) shall be accompanied by the proper fee specified in _____ a) Schedule F b) Schedule G c) Schedule D d) Schedule Z 18. The retailer’s discount shall be _____ of the maximum retail price. a) 12% b) 10% c) 15% d) 18% 19. The re-use of disposable medical devices shall be _____ a) Prohibited b) Selected c) Continued d) Avoided 20. No person shall spend more than _____ of his turnover on advertisement , sampling and other promotional activities in respect of drugs. a) 10% b) 12% c) 50% d) 5%