Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test

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

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

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

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4. Biological and Biotechnological products are included in schedule.

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

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6. TGA is regulatory agency of………….

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

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8. Schedule X of Drugs and Cosmetics Act comprises

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

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

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

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

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13. Pack size of drug is covered under

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14. Schedule J is related to

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

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16. Post marketing surveillance comes under clinical trial

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

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

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19. Example of Schedule G drug is

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

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

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

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

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

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25. Grant of licence to manufacture a drug requires.

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26. In 1954 one of the following act is passed

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

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28. Patent Act is established in

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29. Injection syringe and needles are covered under

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

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31. Dettol comes under

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32. Hatch Waxman Act is related to

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33. Schedule C is related to

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

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35. Aspirin sodium comes under

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36. Purpose of Phase-3 trial is

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

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38. Coca, opium and hemp come under:

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

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40. Drug and Magic Remedies Act is enacted in

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41. Kala jadu or Kavach comes under

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

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43. MCC is regulatory agency of ……………

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

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45. 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

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

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47. MHRA is regulatory agency of ……….....

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

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49. Schedule N states

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

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The average score is 33%

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