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%

__THE END__