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

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

2 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Skin cosmetic preparation

d. Ointment formulation

3 / 50

As per D and C act schedule T stated about

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

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

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

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

4 / 50

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

5 / 50

Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. X

d. B

6 / 50

MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

7 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 3 year

b. Every 5 year

c. Every 2 year

d. Every 6 year

8 / 50

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. All

9 / 50

Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Poisons Act

d. Dangerous Drug Act

10 / 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. Y

c. X

d. V

11 / 50

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

a. Schedule Q

b. Schedule O

c. Schedule P

d. Schedule R

12 / 50

Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule Q

d. Schedule P

13 / 50

Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

14 / 50

Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Ayurvedic drugs

c. Misbranded drugs

d. Toilet preparations

15 / 50

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

a. D

b. FF

c. A

d. Q

16 / 50

For parenteral preparation in glass containers minimum area required is

a. 250 square meters

b. 400 square meters

c. 500 square meters

d. 150 square meters

17 / 50

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. President of India

d. Chief Administrator medical officer of state

18 / 50

Insulin injection according to schedule P is should be stored

a. In cold place

b. At temperature which not exceed 5°C

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

d. At temperature which not exceed 20°C

19 / 50

DTAB has ———————– ex officio members

a. Six

b. Five

c. Four

d. Eight

20 / 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 cool place

d. A Cold place

21 / 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. Adulterated Drug

c. True Drug

d. Misbranded Drug

22 / 50

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

a. H

b. K

c. X

d. G

23 / 50

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

a. Ministry of Education

b. Drug Controller

c. President, Pharmacy Council of India

d. Central Government

24 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of generic drugs

d. List of incurable diseases

25 / 50

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

a. R

b. R1

c. S

d. O

26 / 50

Schedule C is related to

a. List of Biological and Immunological product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Allopathic product

27 / 50

Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Barbital

d. Enalapril

28 / 50

TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. India

d. Denmark

29 / 50

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

a. 2

b. 1

c. 3

d. 4

30 / 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 H

c. Schedule G

d. Schedule I

31 / 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. 21B

d. 20

32 / 50

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

a. White

b. Red

c. Yellow

d. Blue

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

d. Long time adverse effects aster marketing drug

34 / 50

Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Banned drugs

d. Dangerous drugs Act

35 / 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

36 / 50

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

a. 1985

b. 1955

c. 1950

d. 1940

37 / 50

Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule J

d. Schedule P

38 / 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

39 / 50

Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1948

d. 1954

40 / 50

Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 26

d. Form 24

41 / 50

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

a. 500 patients

b. 10-12 patients

c. 1-10 patients

d. 100 patients

42 / 50

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

a. Symbol X given in red

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

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

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

43 / 50

Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

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

d. Standard for cosmetics

44 / 50

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

a. Seven

b. Five

c. Six

d. Nine

45 / 50

MHRA is regulatory agency of ……….....

a. South Africa

b. Brazil

c. Denmark

d. UK

46 / 50

Patent Act is established in

a. 1940

b. 1919

c. 1948

d. 1970

47 / 50

In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. The Medical Termination of pregnancy Act

d. Drug and magic Remedies Act

48 / 50

Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule B

d. Schedule P

49 / 50

Pack size of drug is covered under

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule P1

50 / 50

Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

Your score is

The average score is 38%