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

365

1 / 50

Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Spurious drugs Act

d. Banned drugs

2 / 50

MCC is regulatory agency of ……………

a. UK

b. Brazil

c. South Africa

d. Denmark

3 / 50

Schedule J is related to

a. GMP

b. Pack sizes of drugs.

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

d. Curable disease

4 / 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. In cold place

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

5 / 50

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

a. Schedule J

b. Schedule I

c. Schedule G

d. Schedule H

6 / 50

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

a. Chief Administrator medical officer of state

b. The officer in charge of drugs control organization

c. Government Analyst

d. President of India

7 / 50

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

a. Five

b. Seven

c. Six

d. Nine

8 / 50

Schedule C is related to

a. List of Ayurvedic product

b. List of Biological and Immunological product

c. List of Allopathic product

d. List of Homeopathy product

9 / 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 F

b. Schedule Y

c. Schedule O

d. Schedule M

10 / 50

Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

11 / 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

12 / 50

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

a. Ophthalmic preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Parenteral preparation

13 / 50

Patent Act is established in

a. 1970

b. 1948

c. 1919

d. 1940

14 / 50

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

a. 1

b. 2

c. 4

d. 3

15 / 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

16 / 50

Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Toilet preparations

d. Ayurvedic drugs

17 / 50

Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule Y

d. Schedule H

18 / 50

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

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

b. A cool place

c. Temperature not exceeding 5°C

d. A Cold place

19 / 50

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

a. Symbol X given in red

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

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

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

20 / 50

Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 25

d. Form 24

21 / 50

Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

22 / 50

Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

23 / 50

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

a. 1955

b. 1940

c. 1985

d. 1950

24 / 50

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

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule Q

25 / 50

For parenteral preparation in glass containers minimum area required is

a. 400 square meters

b. 150 square meters

c. 500 square meters

d. 250 square meters

26 / 50

MHRA is regulatory agency of ……….....

a. UK

b. Denmark

c. Brazil

d. South Africa

27 / 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. Spurious Drug

c. True Drug

d. Adulterated Drug

28 / 50

Example of Schedule G drug is

a. Barbital

b. Metformin

c. Cefuroxime

d. Enalapril

29 / 50

TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

30 / 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. Y

c. V

d. W

31 / 50

DTAB has ———————– ex officio members

a. Four

b. Five

c. Six

d. Eight

32 / 50

Injection syringe and needles are covered under

a. Schedule P

b. Schedule B

c. Schedule Q

d. Schedule A

33 / 50

Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule P

d. Schedule O

34 / 50

Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1948

d. 1985

35 / 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 minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

36 / 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

37 / 50

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

a. Q

b. D

c. A

d. FF

38 / 50

In 1954 one of the following act is passed

a. Poisonous Act.

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Narcotic and psychotropic substance Act

39 / 50

Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule P

d. Schedule O

40 / 50

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

a. Blue

b. White

c. Red

d. Yellow

41 / 50

Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase V

d. Phase I

42 / 50

Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

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

d. List of minimum equipment for efficient running of pharmacy

43 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. Guidelines for clinical Trials

d. List of generic drugs

44 / 50

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

a. R1

b. S

c. R

d. O

45 / 50

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

a. H

b. X

c. K

d. G

46 / 50

Schedule D as per D & C Act is concerned with

a. List of prescription drugs

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

c. Requirements of factory premises

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

47 / 50

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

a. 20

b. 21

c. 20B

d. 21B

48 / 50

Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

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

d. Determine Possible therapeutic uses, Effective doses range

49 / 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

50 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

Your score is

The average score is 38%