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1. Purpose of Phase-3 trial is

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

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

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

5. Schedule C is related to

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

7. In 1954 one of the following act is passed

8. Schedule X of Drugs and Cosmetics Act comprises

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

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

11. Drug and Magic Remedies Act is enacted in

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

13. Example of Schedule G drug is

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

15. The schedule in Drug and Cosmetics Act that deals with requirement and guidelines of clinical trial, import and manufacture of new drug is

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

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

18. Schedule J is related to

19. Patent Act is established in

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

21. Injection syringe and needles are covered under

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

23. Schedule N states

24. MCC is regulatory agency of ……………

25. MHRA is regulatory agency of ……….....

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

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

28. Pack size of drug is covered under

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

30. Kala jadu or Kavach comes under

31. 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

32. Dettol comes under

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

34. Aspirin sodium comes under

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

36. As per D and C act schedule T stated about

37. Grant of licence to manufacture a drug requires.

38. For parenteral preparation in glass containers minimum area required is

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

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

41. Hatch Waxman Act is related to

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

43. Post marketing surveillance comes under clinical trial

44. Coca, opium and hemp come under:

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

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

47. TGA is regulatory agency of………….

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

49. Biological and Biotechnological products are included in schedule.

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