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

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 G

d. Schedule J

2 / 50

Purpose of Phase-3 trial is

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

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

c. Determine Possible therapeutic uses, Effective doses range

d. Long time adverse effects aster marketing drug

3 / 50

Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. B

d. A

4 / 50

Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Spurious Drug Act

d. Dangerous Drug Act

5 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 5 year

b. Every 2 year

c. Every 6 year

d. Every 3 year

6 / 50

Patent Act is established in

a. 1940

b. 1948

c. 1919

d. 1970

7 / 50

Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 24

d. Form 25

8 / 50

Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule O

d. Schedule P

9 / 50

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

a. Area for opening retail pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

10 / 50

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

a. President of India

b. Chief Administrator medical officer of state

c. The officer in charge of drugs control organization

d. Government Analyst

11 / 50

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

a. 1-10 patients

b. 10-12 patients

c. 500 patients

d. 100 patients

12 / 50

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

a. Assistant drug controller

b. All

c. Chief pharmacist of government hospital

d. Chief administrative medical officer of the state

13 / 50

Which of the following is prohibited to be imported?

a. Toilet preparations

b. Misbranded drugs

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

14 / 50

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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ophthalmic preparation

d. Ointment formulation

15 / 50

MHRA is regulatory agency of ……….....

a. Brazil

b. UK

c. Denmark

d. South Africa

16 / 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. Adulterated Drug

d. Spurious Drug

17 / 50

MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

18 / 50

As per D and C act schedule T stated about

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

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

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

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

19 / 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

20 / 50

TGA is regulatory agency of………….

a. Zimbabwe

b. Denmark

c. Australia

d. India

21 / 50

Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule P

d. Schedule L

22 / 50

Schedule J is related to

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

b. GMP

c. Curable disease

d. Pack sizes of drugs.

23 / 50

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

a. K

b. X

c. G

d. H

24 / 50

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

a. Ministry of Education

b. Drug Controller

c. Central Government

d. President, Pharmacy Council of India

25 / 50

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

a. D

b. A

c. FF

d. Q

26 / 50

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

a. Temperature not exceeding 5°C

b. A cool place

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

d. A Cold place

27 / 50

Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule A

d. Schedule Q

28 / 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 drug exempted from the provision of import of drugs

d. List of prescription drugs

29 / 50

In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Drug and magic Remedies Act

30 / 50

For parenteral preparation in glass containers minimum area required is

a. 150 square meters

b. 500 square meters

c. 250 square meters

d. 400 square meters

31 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule R

d. Schedule O

32 / 50

Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Banned drugs

d. Spurious drugs Act

33 / 50

Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

34 / 50

DTAB has ———————– ex officio members

a. Five

b. Four

c. Eight

d. Six

35 / 50

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

a. 21

b. 20

c. 20B

d. 21B

36 / 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 N displayed on left top corner of the label.

d. Symbol X given in red

37 / 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 O

b. Schedule F

c. Schedule M

d. Schedule Y

38 / 50

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

a. R1

b. R

c. S

d. O

39 / 50

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

a. Five

b. Six

c. Nine

d. Seven

40 / 50

Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule G

d. Schedule J

41 / 50

Schedule N states

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

b. Standard for cosmetics

c. List of minimum equipment for efficient running of pharmacy

d. Requirement of factory premises and hygienic condition to complied

42 / 50

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

a. 1985

b. 1940

c. 1955

d. 1950

43 / 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. Y

d. W

44 / 50

Drug and Magic Remedies Act is enacted in

a. 1919

b. 1954

c. 1985

d. 1948

45 / 50

Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Metformin

d. Barbital

46 / 50

Insulin injection according to schedule P is should be stored

a. At temperature which not exceed 20°C

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. In cold place

47 / 50

Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule P

d. Schedule O

48 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. List of generic drugs

d. Guidelines for clinical Trials

49 / 50

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

a. Yellow

b. White

c. Blue

d. Red

50 / 50

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

a. 1

b. 3

c. 4

d. 2

Your score is

The average score is 38%