Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test Noteskarts

Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test

This test is Improve for Pharmacy exam like Diploma in Pharmacy exit exam MCQs (DPEE), GPAT, & other competitive exam. Pharmacy Law & Ethics Class Test | Pharmacy Law & Ethics DPEE Test

365

1 / 50

The first edition of India Pharmacopoeia was published in the year :

a. 1985

b. 1955

c. 1940

d. 1950

2 / 50

Schedule D as per D & C Act is concerned with

a. Disease or ailments which a drug may not purport to prevent or cure

b. Requirements of factory premises

c. List of prescription drugs

d. List of drug exempted from the provision of import of drugs

3 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of incurable diseases

d. List of generic drugs

4 / 50

As per D and C Act “Schedule N” is related with

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. List of minimum equipments for efficiently running pharmacy

5 / 50

MCC is regulatory agency of ……………

a. UK

b. Brazil

c. Denmark

d. South Africa

6 / 50

If drug is so colored, coated or polished that damage its therapeutic value or it is made to appear of better or greater therapeutic value than it really is known as

a. Spurious Drug

b. True Drug

c. Misbranded Drug

d. Adulterated Drug

7 / 50

Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. X

d. A

8 / 50

Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Spurious drugs Act

d. Over the counter drugs

9 / 50

State Pharmacy Council should have the following number of elected members.

a. Seven

b. Six

c. Five

d. Nine

10 / 50

Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P1

d. Schedule P

11 / 50

Insulin injection according to schedule P is should be stored

a. At temperature which not exceed 5°C

b. At temperature which not exceed 20°C

c. In cold place

d. At the Temperature 2°C to 8°C and it must not allow to freeze

12 / 50

The schedule in Drug and Cosmetics Act that deals with requirement and guidelines of clinical trial, import and manufacture of new drug is

a. Schedule M

b. Schedule F

c. Schedule Y

d. Schedule O

13 / 50

For schedule X drug use of Human beings special labeling requirement require is

a. Symbol N displayed on left top corner of the label.

b. Symbol X given in red

c. Symbol N is red displayed on left top corner of the label

d. Symbol H displayed on right top corner of the label.

14 / 50

In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

15 / 50

As per D & C Act “Schedule FF” is related with

a. Ophthalmic preparation

b. Ointment formulation

c. Parenteral preparation

d. Skin cosmetic preparation

16 / 50

Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule P

d. Schedule K

17 / 50

Patent Act is established in

a. 1948

b. 1940

c. 1919

d. 1970

18 / 50

Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule G

d. Schedule H

19 / 50

For parenteral preparation in glass containers minimum area required is

a. 150 square meters

b. 250 square meters

c. 500 square meters

d. 400 square meters

20 / 50

Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1954

d. 1919

21 / 50

Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule P

d. Schedule B

22 / 50

The Education Regulation (ER) is published in official gazette by

a. President, Pharmacy Council of India

b. Ministry of Education

c. Drug Controller

d. Central Government

23 / 50

Which of the following is prohibited to be imported?

a. Ayurvedic drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

24 / 50

TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. Denmark

d. India

25 / 50

Schedule C is related to

a. List of Homeopathy product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Allopathic product

26 / 50

Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

d. List of minimum equipment required for manufacturing of drug.

27 / 50

In Phase-2 trial following number of patient should be studied

a. 500 patients

b. 100 patients

c. 10-12 patients

d. 1-10 patients

28 / 50

DTAB has ———————– ex officio members

a. Five

b. Four

c. Six

d. Eight

29 / 50

Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Cefuroxime

d. Barbital

30 / 50

Pro-forma for sending memorandum is included in which schedule?

a. FF

b. Q

c. A

d. D

31 / 50

Standard for mechanical contraceptive comes under Schedule ………………as per D & C Act

a. R

b. S

c. O

d. R1

32 / 50

Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

33 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 3 year

b. Every 5 year

c. Every 2 year

d. Every 6 year

34 / 50

Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase II

d. Phase I

35 / 50

If blood group is “AB” then colour label used is

a. Yellow

b. Blue

c. White

d. Red

36 / 50

List of drugs whole import, manufacture and sale, labeling and packaging are governed by special provisions are included in schedule.

a. X

b. G

c. H

d. K

37 / 50

In State Pharmacy Council all following are ex officio members except.

a. President of India

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. Government Analyst

38 / 50

Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule O

d. Schedule P

39 / 50

Pharmacy Council of India contain comprises…….. Members (s) from AICTE and UGC.

a. 3

b. 4

c. 1

d. 2

40 / 50

Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 26

d. Form 24

41 / 50

List of coal tar colours permitted to be used in cosmetics is covered under.

a. Schedule Q

b. Schedule P

c. Schedule R

d. Schedule O

42 / 50

As per D and C act schedule T stated about

a. Requirements of factory premises for the manufacturer of Homeopathy drugs

b. Requirements of factory premises for the manufacturer of Ayurveda, Sidhha and Unani drugs

c. Requirements of factory premises for the manufacture of Medical device

d. Requirements of factory premises for the manufacturer of Allopathy drugs

43 / 50

One of the following is/all ex officio member(s) of State Pharmacy Council

a. All

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. Chief pharmacist of government hospital

44 / 50

Schedule J is related to

a. List of disease and ailments which drug cannot claim.

b. Curable disease

c. Pack sizes of drugs.

d. GMP

45 / 50

MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Brazil

d. Denmark

46 / 50

For licence granted to sell by retail drugs, specified in schedule C and C(1) drugs from no. require is

a. 21B

b. 20

c. 20B

d. 21

47 / 50

Purpose of Phase-3 trial is

a. To determine maximum tolerated dose in humans, Pharmacodynamics effects, Adverse effect.

b. Long time adverse effects aster marketing drug

c. Determine Possible therapeutic uses, Effective doses range

d. Efficacy and Safety of drug in longer number of patients (500 patients)

48 / 50

As per schedule P Carbenicillin Sodium Powder Should be Stored in/at

a. A Cold place

b. A cool place

c. Temperature not exceeding 5°C

d. Well closed container, protect from light, in cool place, protect from light

49 / 50

List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule I

b. Schedule G

c. Schedule H

d. Schedule J

50 / 50

Schedule…………… of Drugs and Cosmetics Act in Cludes requirements and guidelines on clinical trials for import and manufacturing of new drugs.

a. W

b. X

c. Y

d. V

Your score is

The average score is 38%