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

Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

2 / 50

Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

3 / 50

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

a. FF

b. Q

c. D

d. A

4 / 50

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

a. Ointment formulation

b. Parenteral preparation

c. Skin cosmetic preparation

d. Ophthalmic preparation

5 / 50

Schedule J is related to

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

b. Curable disease

c. GMP

d. Pack sizes of drugs.

6 / 50

Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Banned drugs

d. Spurious drugs Act

7 / 50

Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule N

d. Schedule Q

8 / 50

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

a. 20

b. 20B

c. 21

d. 21B

9 / 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. President of India

d. Government Analyst

10 / 50

Biological and Biotechnological products are included in schedule.

a. A

b. B

c. C and C1

d. X

11 / 50

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

a. 1

b. 4

c. 2

d. 3

12 / 50

Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

13 / 50

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

a. Blue

b. White

c. Yellow

d. Red

14 / 50

Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Metformin

d. Barbital

15 / 50

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

a. Five

b. Six

c. Seven

d. Nine

16 / 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

17 / 50

Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1985

d. 1954

18 / 50

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

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

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 X given in red

19 / 50

Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

20 / 50

Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. List of minimum equipment for efficient running of pharmacy

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

d. Standard for cosmetics

21 / 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 Homeopathy drugs

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

22 / 50

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

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule Q

23 / 50

MHRA is regulatory agency of ……….....

a. UK

b. Denmark

c. Brazil

d. South Africa

24 / 50

For parenteral preparation in glass containers minimum area required is

a. 250 square meters

b. 150 square meters

c. 500 square meters

d. 400 square meters

25 / 50

DTAB has ———————– ex officio members

a. Eight

b. Six

c. Four

d. Five

26 / 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 J

c. Schedule G

d. Schedule I

27 / 50

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

a. O

b. R1

c. S

d. R

28 / 50

Schedule D as per D & C Act is concerned with

a. List of prescription drugs

b. Requirements of factory premises

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

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

29 / 50

TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. India

d. Denmark

30 / 50

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

a. Chief administrative medical officer of the state

b. Chief pharmacist of government hospital

c. Assistant drug controller

d. All

31 / 50

Insulin injection according to schedule P is should be stored

a. At temperature which not exceed 5°C

b. In cold place

c. At temperature which not exceed 20°C

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

32 / 50

Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

33 / 50

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

34 / 50

Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

35 / 50

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

a. G

b. X

c. K

d. H

36 / 50

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

a. 100 patients

b. 500 patients

c. 1-10 patients

d. 10-12 patients

37 / 50

Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase I

d. Phase V

38 / 50

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

a. 1955

b. 1985

c. 1940

d. 1950

39 / 50

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

a. Central Government

b. Ministry of Education

c. Drug Controller

d. President, Pharmacy Council of India

40 / 50

Pharmacy Council of India (PCI) is reconstituted:

a. Every 6 year

b. Every 3 year

c. Every 5 year

d. Every 2 year

41 / 50

Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. List of incurable diseases

d. None of the above

42 / 50

Which of the following is prohibited to be imported?

a. Toilet preparations

b. Ayurvedic drugs

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

43 / 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 Y

c. Schedule M

d. Schedule F

44 / 50

In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. Poisonous Act.

45 / 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

46 / 50

MCC is regulatory agency of ……………

a. Denmark

b. UK

c. South Africa

d. Brazil

47 / 50

Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

48 / 50

Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Poisons Act

49 / 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. Misbranded Drug

d. Spurious Drug

50 / 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. W

c. Y

d. X

Your score is

The average score is 38%