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

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

a. Chief Administrator medical officer of state

b. President of India

c. The officer in charge of drugs control organization

d. Government Analyst

2 / 50

Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

3 / 50

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

a. 3

b. 1

c. 2

d. 4

4 / 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

5 / 50

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

a. 10-12 patients

b. 500 patients

c. 1-10 patients

d. 100 patients

6 / 50

Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Insecticide Act

d. Dangerous Drug Act

7 / 50

For parenteral preparation in glass containers minimum area required is

a. 500 square meters

b. 150 square meters

c. 250 square meters

d. 400 square meters

8 / 50

Biological and Biotechnological products are included in schedule.

a. A

b. B

c. C and C1

d. X

9 / 50

Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule J

d. Schedule P

10 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. Area for opening retail pharmacy

11 / 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

12 / 50

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

a. R

b. O

c. R1

d. S

13 / 50

DTAB has ———————– ex officio members

a. Six

b. Eight

c. Four

d. Five

14 / 50

Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 25

d. Form 24

15 / 50

Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase III

d. Phase II

16 / 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. At temperature which not exceed 5°C

c. In cold place

d. At temperature which not exceed 20°C

17 / 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 Allopathy drugs

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

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

18 / 50

Patent Act is established in

a. 1948

b. 1919

c. 1940

d. 1970

19 / 50

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

a. A

b. D

c. Q

d. FF

20 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 3 year

b. Every 6 year

c. Every 5 year

d. Every 2 year

21 / 50

Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

22 / 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

23 / 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. Spurious Drug

c. Misbranded Drug

d. Adulterated Drug

24 / 50

Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule P

d. Schedule O

25 / 50

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

a. Seven

b. Six

c. Five

d. Nine

26 / 50

Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule N

d. Schedule P

27 / 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

28 / 50

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

a. 1950

b. 1940

c. 1955

d. 1985

29 / 50

Schedule…………… of Drugs and Cosmetics Act in Cludes requirements and guidelines on clinical trials for import and manufacturing of new drugs.

a. V

b. X

c. Y

d. W

30 / 50

In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

31 / 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

32 / 50

Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

33 / 50

Schedule D as per D & C Act is concerned with

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

b. Requirements of factory premises

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

d. List of prescription drugs

34 / 50

Schedule J is related to

a. Pack sizes of drugs.

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

c. GMP

d. Curable disease

35 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Parenteral preparation

d. Ointment formulation

36 / 50

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

a. Schedule P

b. Schedule O

c. Schedule Q

d. Schedule R

37 / 50

MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

38 / 50

MHRA is regulatory agency of ……….....

a. South Africa

b. Denmark

c. Brazil

d. UK

39 / 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 X given in red

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

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

40 / 50

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

a. Central Government

b. Drug Controller

c. Ministry of Education

d. President, Pharmacy Council of India

41 / 50

Which of the following is prohibited to be imported?

a. Toilet preparations

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

42 / 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 O

d. Schedule M

43 / 50

Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule B

d. Schedule P

44 / 50

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

a. 21

b. 20B

c. 21B

d. 20

45 / 50

Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

46 / 50

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

a. Yellow

b. White

c. Blue

d. Red

47 / 50

Schedule N states

a. Standard for cosmetics

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

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

48 / 50

Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Allopathic product

49 / 50

Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Dangerous drugs Act

d. Banned drugs

50 / 50

TGA is regulatory agency of………….

a. Zimbabwe

b. India

c. Australia

d. Denmark

Your score is

The average score is 38%