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

358

1 / 50

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

a. Schedule J

b. Schedule G

c. Schedule H

d. Schedule I

2 / 50

2. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Denmark

d. Brazil

3 / 50

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

4 / 50

4. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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

a. Requirements of factory premises

b. List of prescription drugs

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

6 / 50

6. 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 N displayed on left top corner of the label.

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

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

a. 4

b. 3

c. 1

d. 2

8 / 50

8. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 27

d. Form 25

9 / 50

9. 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

10 / 50

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

a. H

b. K

c. X

d. G

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11. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Cefuroxime

d. Metformin

12 / 50

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

a. D

b. A

c. FF

d. Q

13 / 50

13. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

14 / 50

14. 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 F

b. Schedule O

c. Schedule Y

d. Schedule M

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15. 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. 21B

d. 20B

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

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule Q

17 / 50

17. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Spurious Drug Act

d. Poisons Act

18 / 50

18. 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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19. 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

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20. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Brazil

d. Denmark

21 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

22 / 50

22. 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

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23. 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. Misbranded Drug

b. Adulterated Drug

c. Spurious Drug

d. True Drug

24 / 50

24. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

25 / 50

25. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule P

d. Schedule A

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26. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of incurable diseases

d. List of generic drugs

27 / 50

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

a. Nine

b. Five

c. Seven

d. Six

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

a. Chief Administrator medical officer of state

b. President of India

c. Government Analyst

d. The officer in charge of drugs control organization

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29. TGA is regulatory agency of………….

a. India

b. Australia

c. Zimbabwe

d. Denmark

30 / 50

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

a. Four

b. Five

c. Eight

d. Six

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31. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

32 / 50

32. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

33 / 50

33. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. A

d. C and C1

34 / 50

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

a. 100 patients

b. 1-10 patients

c. 500 patients

d. 10-12 patients

35 / 50

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

a. Red

b. White

c. Yellow

d. Blue

36 / 50

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

a. O

b. R

c. S

d. R1

37 / 50

37. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Dangerous drugs Act

d. Spurious drugs Act

38 / 50

38. Patent Act is established in

a. 1948

b. 1940

c. 1919

d. 1970

39 / 50

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

a. 1940

b. 1950

c. 1985

d. 1955

40 / 50

40. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

41 / 50

41. 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

42 / 50

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

a. Drug Controller

b. Central Government

c. Ministry of Education

d. President, Pharmacy Council of India

43 / 50

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

a. In cold place

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

c. At temperature which not exceed 5°C

d. At temperature which not exceed 20°C

44 / 50

44. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

45 / 50

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

a. A cool place

b. A Cold place

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

d. Temperature not exceeding 5°C

46 / 50

46. 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

47 / 50

47. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

48 / 50

48. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase V

d. Phase III

49 / 50

49. 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.

50 / 50

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

a. Every 6 year

b. Every 5 year

c. Every 3 year

d. Every 2 year

Your score is

The average score is 37%