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

a. FF

b. Q

c. D

d. A

2 / 50

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

a. White

b. Red

c. Yellow

d. Blue

3 / 50

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

a. Central Government

b. President, Pharmacy Council of India

c. Drug Controller

d. Ministry of Education

4 / 50

4. Schedule J is related to

a. Pack sizes of drugs.

b. Curable disease

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

d. GMP

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5. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. A

d. X

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

a. Eight

b. Five

c. Four

d. Six

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

a. 150 square meters

b. 500 square meters

c. 400 square meters

d. 250 square meters

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8. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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9. 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 X given in red

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

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

a. Requirements of factory premises

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. List of prescription drugs

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

a. Every 6 year

b. Every 5 year

c. Every 3 year

d. Every 2 year

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

a. 20B

b. 21

c. 21B

d. 20

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13. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. All

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15. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

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16. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase II

d. Phase I

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17. TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. Denmark

d. India

18 / 50

18. Patent Act is established in

a. 1948

b. 1919

c. 1970

d. 1940

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

20 / 50

20. 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 Homeopathy drugs

c. Requirements of factory premises for the manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

a. Y

b. X

c. V

d. W

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

a. K

b. G

c. H

d. X

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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ointment formulation

d. Ophthalmic preparation

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

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule R

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25. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. Denmark

d. UK

26 / 50

26. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

27 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Misbranded drugs

28 / 50

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

a. Six

b. Seven

c. Nine

d. Five

29 / 50

29. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

30 / 50

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

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

a. A cool place

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

c. Temperature not exceeding 5°C

d. A Cold place

32 / 50

32. 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 M

c. Schedule Y

d. Schedule F

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33. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

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

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule I

35 / 50

35. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule P

d. Schedule O

36 / 50

36. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

37 / 50

37. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of generic drugs

d. List of incurable diseases

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38. Hatch Waxman Act is related to

a. Banned drugs

b. Dangerous drugs Act

c. Over the counter drugs

d. Spurious drugs Act

39 / 50

39. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule O

d. Schedule R

40 / 50

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

a. At temperature which not exceed 20°C

b. In cold place

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

d. At temperature which not exceed 5°C

41 / 50

41. 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. Spurious Drug

d. Misbranded Drug

42 / 50

42. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

43 / 50

43. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Metformin

d. Cefuroxime

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

a. 2

b. 1

c. 3

d. 4

45 / 50

45. Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule A

d. Schedule Q

46 / 50

46. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

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

a. 1940

b. 1950

c. 1955

d. 1985

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48. 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

49 / 50

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

a. O

b. R1

c. R

d. S

50 / 50

50. Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule H

d. Schedule Y

Your score is

The average score is 37%