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

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. Determine Possible therapeutic uses, Effective doses range

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

2 / 50

Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

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

d. Requirement of factory premises and hygienic condition to complied

3 / 50

For parenteral preparation in glass containers minimum area required is

a. 500 square meters

b. 250 square meters

c. 400 square meters

d. 150 square meters

4 / 50

Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase III

d. Phase II

5 / 50

Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Metformin

d. Barbital

6 / 50

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

a. Y

b. X

c. W

d. V

7 / 50

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

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

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

c. Symbol X given in red

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

8 / 50

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

a. Area for opening retail pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

9 / 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. True Drug

b. Misbranded Drug

c. Spurious Drug

d. Adulterated Drug

10 / 50

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

a. Seven

b. Six

c. Five

d. Nine

11 / 50

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

a. Schedule Q

b. Schedule O

c. Schedule R

d. Schedule P

12 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. None of the above

d. Guidelines for clinical Trials

13 / 50

In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. Drug and magic Remedies Act

14 / 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 5°C

c. In cold place

d. At temperature which not exceed 20°C

15 / 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. K

d. H

16 / 50

Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Banned drugs

d. Spurious drugs Act

17 / 50

Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

18 / 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

19 / 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 O

c. Schedule F

d. Schedule M

20 / 50

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

a. 4

b. 1

c. 2

d. 3

21 / 50

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

a. Schedule H

b. Schedule I

c. Schedule J

d. Schedule G

22 / 50

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

a. Blue

b. Yellow

c. White

d. Red

23 / 50

Schedule D as per D & C Act is concerned with

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

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

c. Requirements of factory premises

d. List of prescription drugs

24 / 50

Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule N

d. Schedule O

25 / 50

Schedule J is related to

a. GMP

b. Curable disease

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

d. Pack sizes of drugs.

26 / 50

Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Ayurvedic product

27 / 50

Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule P

d. Schedule L

28 / 50

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

a. O

b. R

c. R1

d. S

29 / 50

MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

30 / 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

31 / 50

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

a. Parenteral preparation

b. Ophthalmic preparation

c. Skin cosmetic preparation

d. Ointment formulation

32 / 50

DTAB has ———————– ex officio members

a. Four

b. Five

c. Six

d. Eight

33 / 50

Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule A

d. Schedule B

34 / 50

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

a. 1955

b. 1950

c. 1940

d. 1985

35 / 50

TGA is regulatory agency of………….

a. Australia

b. Zimbabwe

c. India

d. Denmark

36 / 50

MHRA is regulatory agency of ……….....

a. Brazil

b. South Africa

c. Denmark

d. UK

37 / 50

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

a. Drug Controller

b. Ministry of Education

c. President, Pharmacy Council of India

d. Central Government

38 / 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 Homeopathy drugs

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

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

39 / 50

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

a. 10-12 patients

b. 500 patients

c. 100 patients

d. 1-10 patients

40 / 50

Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Ayurvedic drugs

d. Toilet preparations

41 / 50

Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule P1

42 / 50

Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. X

d. B

43 / 50

Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

44 / 50

Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule G

d. Schedule H

45 / 50

Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

46 / 50

Patent Act is established in

a. 1919

b. 1940

c. 1948

d. 1970

47 / 50

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

a. Government Analyst

b. Chief Administrator medical officer of state

c. President of India

d. The officer in charge of drugs control organization

48 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 2 year

b. Every 3 year

c. Every 5 year

d. Every 6 year

49 / 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. Chief pharmacist of government hospital

d. All

50 / 50

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

a. FF

b. A

c. Q

d. D

Your score is

The average score is 38%