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

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

a. Parenteral preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Skin cosmetic preparation

2 / 50

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

a. Chief pharmacist of government hospital

b. All

c. Chief administrative medical officer of the state

d. Assistant drug controller

3 / 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

4 / 50

Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Metformin

d. Cefuroxime

5 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. Area for opening retail pharmacy

d. List of maximum equipments for efficiently running pharmacy

6 / 50

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

a. Red

b. White

c. Blue

d. Yellow

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

d. Determine Possible therapeutic uses, Effective doses range

8 / 50

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

a. Schedule G

b. Schedule I

c. Schedule H

d. Schedule J

9 / 50

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

a. K

b. G

c. H

d. X

10 / 50

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

a. 21B

b. 21

c. 20

d. 20B

11 / 50

Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule H

d. Schedule G

12 / 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 M

c. Schedule F

d. Schedule Y

13 / 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. In cold place

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

14 / 50

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

a. Q

b. D

c. A

d. FF

15 / 50

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

a. Drug Controller

b. Central Government

c. President, Pharmacy Council of India

d. Ministry of Education

16 / 50

Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Spurious drugs Act

d. Dangerous drugs Act

17 / 50

Biological and Biotechnological products are included in schedule.

a. B

b. A

c. C and C1

d. X

18 / 50

DTAB has ———————– ex officio members

a. Six

b. Four

c. Eight

d. Five

19 / 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

20 / 50

Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

21 / 50

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

a. O

b. S

c. R1

d. R

22 / 50

MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. UK

d. Brazil

23 / 50

Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Spurious Drug Act

d. Dangerous Drug Act

24 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

25 / 50

In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Poisonous Act.

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

26 / 50

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

a. President of India

b. Government Analyst

c. Chief Administrator medical officer of state

d. The officer in charge of drugs control organization

27 / 50

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

a. 2

b. 3

c. 1

d. 4

28 / 50

Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

29 / 50

Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

30 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 2 year

b. Every 3 year

c. Every 5 year

d. Every 6 year

31 / 50

Schedule D as per D & C Act is concerned with

a. Requirements of factory premises

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

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

d. List of prescription drugs

32 / 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. Adulterated Drug

b. True Drug

c. Spurious Drug

d. Misbranded Drug

33 / 50

Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Ayurvedic drugs

c. Toilet preparations

d. Misbranded drugs

34 / 50

Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule O

d. Schedule N

35 / 50

Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule L

d. Schedule J

36 / 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

37 / 50

MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

38 / 50

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

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule R

39 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. List of generic drugs

c. None of the above

d. Guidelines for clinical Trials

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

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

41 / 50

Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

42 / 50

TGA is regulatory agency of………….

a. Denmark

b. India

c. Zimbabwe

d. Australia

43 / 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

44 / 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

45 / 50

Patent Act is established in

a. 1919

b. 1970

c. 1948

d. 1940

46 / 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 Allopathy drugs

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

47 / 50

Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1954

d. 1948

48 / 50

Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule R

d. Schedule O

49 / 50

Schedule J is related to

a. Curable disease

b. GMP

c. Pack sizes of drugs.

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

50 / 50

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

a. Seven

b. Six

c. Nine

d. Five

Your score is

The average score is 38%