GPAT Important Question Subject: Pharmaceutical Jurisprudence

 

***********************************************************************

GPAT Important Question

Subject: Pharmaceutical Jurisprudence

Question Paper with Answer  

***********************************************************************

1.  If it consists, in whole or in part, of any filthy, putrid, or decomposed substance is called as

a.       Spurious Drugs

b.      Adulterated Drugs

c.       Misbranded Drugs

d.      None of the above

2.      A drug shall be deemed to be ……………….: (i) If it is manufactured under a name which belongs to another drug.

a.       Spurious Drugs

b.      Spurious cosmetics 

c.       Misbranded Drugs

d.      Misbranded Cosmetics

3.      DTAB………….

a.       Drug Transport Advisory Board

b.      Drug Transparency Advisory Board

c.       Drug Technical Advisory Board

d.      Drug Technology Advisory Board

4.      Fee structure for drug analysis by Central Drug Laboratory or by the Govt. Analyst given in

a.       Schedule A

b.      Schedule B

c.       Schedule C

d.      Schedule F

5.      Standards of surgical dressings

a.       Schedule F

b.      Schedule F1

c.       Schedule F2

d.      Schedule F3

6.      Life Period of drugs given in ……….

a.       Days

b.      Weeks

c.       Months

d.      Years

7.      BSI…….

a.       Bureau of Indian Standards

b.      Bureau of Italian Standards

c.       Bureau of Internet Standards

d.      Noe of Above

8.      Standards for condoms……

a.       Schedule R1

b.      Schedule T

c.       Schedule R

d.      Schedule U

9.      Requirement and guidelines for clinical trials given in schedule

a.       H

b.      G

c.       M

d.      Y

10.  Mercaptopurine belong to

a.       Schedule G

b.      Schedule H

c.       Schedule K

d.      Schedule W

11.   Narcotic Drugs and Psychotropic Substances Act, established in…….

a.       1995

b.      2003

c.       1975

d.      1985

12.  The drug label must display the texts "…….." on the left top corner of the Schedule H drug.

a.       NRx

b.      RNx

c.       Rx

d.      Xr

13.  Requirements for factory premises for the manufacture of cosmetics given in….

a.       Schedule M

b.      Schedule M1

c.       Schedule M2

d.      Schedule M3

14.   Cool place means,

a.       a temperature of 15-25°c

b.      a temperature of 25-30°c

c.       a temperature of 0-8°c

d.      a temperature of 10-25°c

15.  Albendazole suspension comes in pack of……

a.       05 mL

b.      10 mL

c.       20 mL

d.      25 mL

16.   I.U. ….

a.       Indian Units

b.      Interchange unit

c.       International units

d.      None of above

17.   All belove drugs are schedule X Drug Except:

a.       Secobarbital,

b.      Glutethimide,

c.       Cyclobarbital

d.      Paracetamol

18.  For getting license of Wholesale, area shall not be less than.

a.       20 Sq. mt

b.      05 sq. mt

c.       10 Sq. mt

d.      None of above

19.  Dispensing department shall be not less than 6 sq. m. for one pharmacist working therein with additional ………. for 2 additional pharmacists.

a.       2 sq. m.

b.      4 sq. m.

c.       6 sq. m.

d.      8 sq. m.

20.   Separate cupboards with lock and key for Poisons and shall be marked in ………. letters as ‘’POISON’’ on a white background.

a.       Red

b.      Blue

c.       Black

d.      Danger

21.   Minimum area required for setting up Ayurveda, Sidha and Unani Medicine manufacturing unit is …………. covered with separate cabins and partitions for each activity.

a.       1100 sq. ft.

b.      1150 sq. ft.

c.       1250 sq. ft.

d.      1200 sq. ft.

22.    For getting Restricted type license required which of the following from

a.       20-A

b.      20-B

c.       21-A

d.       a & c

23.   Sale or distribution of Without a license penalty for subsequent conviction

a.       Imprisonment for not less than 2 years or fine up to 10,000.

b.      Imprisonment for not less than 1 years or fine up to 5,000.

c.       Imprisonment for not less than 4 years or fine unto 10,000.

d.       B and C

24.  Central Government established a Central Drugs Laboratory under the control of a ……….to be appointed by the Central Government

a.       Scientist

b.      Chairman

c.       Director

d.      None of above

25.   Central Drugs Laboratory is in……

a.       Kolkata

b.      Chennai

c.        Mumbai

d.      Gazipur

26.   First Chemist Shop introduced in India in….

a.       1811

b.      1821

c.       1911

d.      None of above

27.   Government of India, appointed The Drug Enquiry Committee on

a.       11th August 1930

b.      12th August 1930

c.       13th August 1930

d.      14th August 1930

28.  Sir Joseph Bhore was chairmanship of….

a.       HEALTH SURVEY AND DEVELOPMENT COMMITTEE

b.      MUDLIAR COMMITTEE

c.       DCC

d.      DTAB

29.  Dr. A. Lakshmanswamy Mudliar and this committee was also known as

a.       Health survey and development committee

b.      Drug Consultative Committee

c.       Health Survey and Planning Committee

d.      None of above

30.  HATHI COMMITTEE was set up under the Chairmanship of Jaisukh Lal Hathi for covered all aspects ranging from

a.       licensing, price control, imports,

b.      the role of the foreign sector,

c.       quality control

d.      All

31.  THE PHARMACY ACT, 1948 passes on

a.       6 March 1948

b.      8 March 1948

c.       4 March 1948

d.      10 Feb 1948

32.  Ethics is …… principles

a.       Moral

b.      Immoral

c.       Dishonest

d.      None of above

33.  Hawking of drugs and medicinal should not be encouraged nor should any attempt be made to solicit orders for such substances from……..

a.       Doctor to Doctor

b.      Medical to Medical

c.       Door to Door

d.      None of above

34.  No certificate or credentials should be granted unless the above criterion is attained and the recipient has proved himself worthy of the same to…..

a.       Registered pharmacist

b.      Pharmacist

c.       Apprentice Pharmacist

d.      None of above

35.  A pharmacist should always use drugs and medicinal preparations of   

a.       standard Poor quality

b.      Substandard drug

c.       Standard quality

d.      None of above

36.  MUDLIAR COMMITTEE was appointed in

a.       June 1959

b.      October 1943

c.       June 1954

d.      October 1948

37.  Director General of Health Services, who shall be ………… of   DTAB

a.       Chairman

b.      President

c.       Director

d.      None of above

38.   Schedule-X drugs, Retail, license form………

a.       20-F

b.      20-G

c.       21-F

d.      21-F

39.  The statement “use the solution within one month after opening the container”. Related to ophthalmic preparation given in schedule

a.       Schedule FF

b.      Schedule F

c.       Schedule F1

d.      Schedule F2

40.  Drug Control laboratory in Baroda, Bhuj, Rajkot, in respective years, 1959, 1979, ……….

a.       1983

b.      1993

c.       2003

d.      1973 

**************************************************************************