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. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

2 / 50

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

a. 1985

b. 1940

c. 1950

d. 1955

3 / 50

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

a. Four

b. Eight

c. Five

d. Six

4 / 50

4. 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 manufacturer of Homeopathy drugs

c. Requirements of factory premises for the manufacture of Medical device

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

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5. Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

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

d. Requirement of factory premises and hygienic condition to complied

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

a. 3

b. 4

c. 1

d. 2

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

a. Nine

b. Six

c. Five

d. Seven

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

a. Area for opening retail pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

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9. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1985

d. 1948

10 / 50

10. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

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12. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

13 / 50

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

a. Requirements of factory premises

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

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

d. List of prescription drugs

14 / 50

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

a. S

b. R1

c. O

d. R

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15. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. None of the above

d. List of incurable diseases

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16. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

17 / 50

17. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

18 / 50

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

a. Schedule R

b. Schedule Q

c. Schedule P

d. Schedule O

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

a. Temperature not exceeding 5°C

b. A cool place

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

d. A Cold place

20 / 50

20. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule Y

d. Schedule H

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21. 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. True Drug

d. Adulterated Drug

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22. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

23 / 50

23. TGA is regulatory agency of………….

a. India

b. Denmark

c. Zimbabwe

d. Australia

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24. 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

25 / 50

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

a. Ministry of Education

b. Drug Controller

c. President, Pharmacy Council of India

d. Central Government

26 / 50

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

a. Chief pharmacist of government hospital

b. Assistant drug controller

c. All

d. Chief administrative medical officer of the state

27 / 50

27. 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 I

c. Schedule H

d. Schedule G

28 / 50

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

a. Symbol X given in red

b. Symbol N displayed on left top corner of the label.

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

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

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29. Schedule J is related to

a. Curable disease

b. GMP

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

d. Pack sizes of drugs.

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30. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule Q

d. Schedule N

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

a. 1-10 patients

b. 100 patients

c. 500 patients

d. 10-12 patients

32 / 50

32. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. X

d. B

33 / 50

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

34 / 50

34. Pack size of drug is covered under

a. Schedule O

b. Schedule R

c. Schedule P1

d. Schedule P

35 / 50

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

a. Red

b. Blue

c. Yellow

d. White

36 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

37 / 50

37. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule A

d. Schedule B

38 / 50

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

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

b. At temperature which not exceed 5°C

c. In cold place

d. At temperature which not exceed 20°C

39 / 50

39. Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Barbital

d. Enalapril

40 / 50

40. 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 F

d. Schedule Y

41 / 50

41. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

42 / 50

42. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Biological and Immunological product

43 / 50

43. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Banned drugs

d. Spurious drugs Act

44 / 50

44. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule K

d. Schedule J

45 / 50

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

a. Q

b. D

c. A

d. FF

46 / 50

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

a. 150 square meters

b. 500 square meters

c. 250 square meters

d. 400 square meters

47 / 50

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

a. 20

b. 21B

c. 20B

d. 21

48 / 50

48. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. Poisonous Act.

49 / 50

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. President of India

50 / 50

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

a. W

b. Y

c. V

d. X

Your score is

The average score is 37%