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

Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

2 / 50

Which of the following is prohibited to be imported?

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Ayurvedic drugs

3 / 50

Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

4 / 50

Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

5 / 50

Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

6 / 50

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

a. 1-10 patients

b. 500 patients

c. 10-12 patients

d. 100 patients

7 / 50

Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule Y

d. Schedule J

8 / 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 H displayed on right top corner of the label.

c. Symbol X given in red

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

9 / 50

Schedule D as per D & C Act is concerned with

a. List of prescription drugs

b. Requirements of factory premises

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

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

10 / 50

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

a. Temperature not exceeding 5°C

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

c. A Cold place

d. A cool place

11 / 50

Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Spurious drugs Act

d. Banned drugs

12 / 50

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

a. White

b. Blue

c. Red

d. Yellow

13 / 50

Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

14 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. List of incurable diseases

d. None of the above

15 / 50

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

a. K

b. H

c. G

d. X

16 / 50

MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. South Africa

d. UK

17 / 50

Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

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

d. GMP

18 / 50

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

a. Chief Administrator medical officer of state

b. President of India

c. Government Analyst

d. The officer in charge of drugs control organization

19 / 50

Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

20 / 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

21 / 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 Y

b. Schedule M

c. Schedule O

d. Schedule F

22 / 50

As per D and C act schedule T stated about

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

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

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

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

23 / 50

Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 27

c. Form 25

d. Form 26

24 / 50

Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Barbital

d. Metformin

25 / 50

Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Biological and Immunological product

26 / 50

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

a. Ointment formulation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Parenteral preparation

27 / 50

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

a. D

b. Q

c. FF

d. A

28 / 50

Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Poisons Act

c. Spurious Drug Act

d. Insecticide Act

29 / 50

For parenteral preparation in glass containers minimum area required is

a. 250 square meters

b. 400 square meters

c. 150 square meters

d. 500 square meters

30 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule O

d. Schedule R

31 / 50

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

a. Assistant drug controller

b. Chief administrative medical officer of the state

c. All

d. Chief pharmacist of government hospital

32 / 50

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

a. O

b. R1

c. S

d. R

33 / 50

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

a. 1985

b. 1955

c. 1940

d. 1950

34 / 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 J

c. Schedule H

d. Schedule G

35 / 50

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

a. Drug Controller

b. Ministry of Education

c. Central Government

d. President, Pharmacy Council of India

36 / 50

Insulin injection according to schedule P is should be stored

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

b. At temperature which not exceed 20°C

c. At temperature which not exceed 5°C

d. In cold place

37 / 50

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

a. 4

b. 3

c. 1

d. 2

38 / 50

DTAB has ———————– ex officio members

a. Six

b. Four

c. Eight

d. Five

39 / 50

TGA is regulatory agency of………….

a. Denmark

b. Australia

c. Zimbabwe

d. India

40 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 5 year

b. Every 6 year

c. Every 2 year

d. Every 3 year

41 / 50

MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Denmark

d. Brazil

42 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

43 / 50

In 1954 one of the following act is passed

a. Poisonous Act.

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

44 / 50

Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

45 / 50

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

a. 21B

b. 21

c. 20B

d. 20

46 / 50

Drug and Magic Remedies Act is enacted in

a. 1919

b. 1954

c. 1948

d. 1985

47 / 50

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

a. Nine

b. Seven

c. Six

d. Five

48 / 50

Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule B

d. Schedule Q

49 / 50

Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

50 / 50

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

a. X

b. W

c. Y

d. V

Your score is

The average score is 38%