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

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1 / 50

1. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Cefuroxime

d. Barbital

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2. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

3 / 50

3. 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

4 / 50

4. Which of the following is prohibited to be imported?

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Ayurvedic drugs

5 / 50

5. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

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6. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. None of the above

d. List of incurable diseases

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7. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1948

c. 1954

d. 1919

8 / 50

8. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule O

d. Schedule R

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9. 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

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

a. All

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. Assistant drug controller

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

a. Yellow

b. Red

c. White

d. Blue

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

a. President of India

b. The officer in charge of drugs control organization

c. Government Analyst

d. Chief Administrator medical officer of state

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13. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase II

d. Phase I

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

a. 1940

b. 1985

c. 1955

d. 1950

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15. Pharmacy Council of India (PCI) is reconstituted:

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

16 / 50

16. Patent Act is established in

a. 1919

b. 1970

c. 1940

d. 1948

17 / 50

17. Injection syringe and needles are covered under

a. Schedule P

b. Schedule B

c. Schedule Q

d. Schedule A

18 / 50

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

a. FF

b. D

c. Q

d. A

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19. 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.

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

a. O

b. R

c. S

d. R1

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

a. Nine

b. Six

c. Seven

d. Five

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22. MHRA is regulatory agency of ……….....

a. South Africa

b. Denmark

c. UK

d. Brazil

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23. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Ophthalmic preparation

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25. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

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

a. W

b. V

c. X

d. Y

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

a. Schedule I

b. Schedule H

c. Schedule G

d. Schedule J

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28. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

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29. Schedule D as per D & C Act is concerned with

a. List of prescription drugs

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

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

d. Requirements of factory premises

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30. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

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31. 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. H

d. G

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32. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Poisons Act

c. Insecticide Act

d. Spurious Drug Act

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33. 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. 21B

d. 21

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34. Schedule C is related to

a. List of Biological and Immunological product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Allopathic product

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Central Government

d. Drug Controller

36 / 50

36. 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. Temperature not exceeding 5°C

c. A Cold place

d. A cool place

37 / 50

37. 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

38 / 50

38. DTAB has ———————– ex officio members

a. Four

b. Five

c. Six

d. Eight

39 / 50

39. Insulin injection according to schedule P is should be stored

a. At temperature which not exceed 20°C

b. In cold place

c. At temperature which not exceed 5°C

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

40 / 50

40. 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

41 / 50

41. TGA is regulatory agency of………….

a. Zimbabwe

b. Denmark

c. India

d. Australia

42 / 50

42. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. UK

d. Denmark

43 / 50

43. 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

44 / 50

44. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Dangerous drugs Act

d. Banned drugs

45 / 50

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

a. 1

b. 4

c. 2

d. 3

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46. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Poisonous Act.

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47. 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 H displayed on right top corner of the label.

c. Symbol X given in red

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

48 / 50

48. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule H

d. Schedule J

49 / 50

49. 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

50 / 50

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. Misbranded Drug

c. Adulterated Drug

d. True Drug

Your score is

The average score is 37%