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

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

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

Top 50 Question for Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law and Ethics DPEE

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1 / 50

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

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

2 / 50

DTAB has ———————– ex officio members

a. Four

b. Six

c. Eight

d. Five

3 / 50

MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

4 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 6 year

b. Every 3 year

c. Every 2 year

d. Every 5 year

5 / 50

Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

6 / 50

Insulin injection according to schedule P is should be stored

a. At temperature which not exceed 5°C

b. In cold place

c. At temperature which not exceed 20°C

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

7 / 50

Schedule J is related to

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

b. Pack sizes of drugs.

c. GMP

d. Curable disease

8 / 50

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

9 / 50

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

a. Skin cosmetic preparation

b. Ophthalmic preparation

c. Parenteral preparation

d. Ointment formulation

10 / 50

Schedule D as per D & C Act is concerned with

a. Requirements of factory premises

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

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

d. List of prescription drugs

11 / 50

Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule K

d. Schedule L

12 / 50

Schedule C is related to

a. List of Ayurvedic product

b. List of Biological and Immunological product

c. List of Homeopathy product

d. List of Allopathic product

13 / 50

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. President of India

d. The officer in charge of drugs control organization

14 / 50

Patent Act is established in

a. 1919

b. 1970

c. 1940

d. 1948

15 / 50

Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Ayurvedic drugs

c. Misbranded drugs

d. Toilet preparations

16 / 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

17 / 50

Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule G

d. Schedule Y

18 / 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. V

c. W

d. Y

19 / 50

Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

20 / 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 manufacture of Medical device

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

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

21 / 50

Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

22 / 50

Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Metformin

d. Barbital

23 / 50

For parenteral preparation in glass containers minimum area required is

a. 250 square meters

b. 150 square meters

c. 400 square meters

d. 500 square meters

24 / 50

TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

25 / 50

Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

26 / 50

MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

27 / 50

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

a. G

b. K

c. X

d. H

28 / 50

Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P1

d. Schedule P

29 / 50

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

a. Six

b. Nine

c. Five

d. Seven

30 / 50

Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Insecticide Act

31 / 50

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

a. White

b. Blue

c. Yellow

d. Red

32 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

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

d. A cool place

33 / 50

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

a. 3

b. 4

c. 2

d. 1

34 / 50

Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. List of minimum equipment for efficient running of pharmacy

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

d. Standard for cosmetics

35 / 50

Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1985

d. 1948

36 / 50

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

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule Q

37 / 50

In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Poisonous Act.

c. The Medical Termination of pregnancy Act

d. Drug and magic Remedies Act

38 / 50

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

a. All

b. Assistant drug controller

c. Chief administrative medical officer of the state

d. Chief pharmacist of government hospital

39 / 50

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

a. Q

b. FF

c. A

d. D

40 / 50

Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule O

d. Schedule P

41 / 50

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

a. 20B

b. 21

c. 20

d. 21B

42 / 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 G

c. Schedule I

d. Schedule J

43 / 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. Misbranded Drug

b. True Drug

c. Adulterated Drug

d. Spurious Drug

44 / 50

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

a. 100 patients

b. 1-10 patients

c. 500 patients

d. 10-12 patients

45 / 50

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

a. R

b. R1

c. S

d. O

46 / 50

Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

47 / 50

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

a. 1940

b. 1950

c. 1955

d. 1985

48 / 50

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

a. Ministry of Education

b. Central Government

c. Drug Controller

d. President, Pharmacy Council of India

49 / 50

Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase V

d. Phase III

50 / 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 F

c. Schedule M

d. Schedule O

Your score is

The average score is 38%