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

330

1 / 50

1. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

2 / 50

2. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule K

d. Schedule L

3 / 50

3. 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. Misbranded Drug

c. Spurious Drug

d. True Drug

4 / 50

4. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

5 / 50

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

a. At temperature which not exceed 5°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 20°C

6 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

7 / 50

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

a. R

b. R1

c. O

d. S

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8. Pack size of drug is covered under

a. Schedule O

b. Schedule P1

c. Schedule R

d. Schedule P

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9. Schedule N states

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

b. Standard for cosmetics

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

10 / 50

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

a. FF

b. D

c. Q

d. A

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

a. 500 patients

b. 1-10 patients

c. 10-12 patients

d. 100 patients

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

a. 1

b. 3

c. 2

d. 4

13 / 50

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

a. 20B

b. 20

c. 21

d. 21B

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14. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

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

a. List of prescription drugs

b. Requirements of factory premises

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

16 / 50

16. Dettol comes under

a. Schedule Q

b. Schedule O

c. Schedule N

d. Schedule P

17 / 50

17. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. X

d. B

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

a. 400 square meters

b. 500 square meters

c. 250 square meters

d. 150 square meters

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19. Patent Act is established in

a. 1940

b. 1919

c. 1948

d. 1970

20 / 50

20. 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. X

d. H

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

a. Chief administrative medical officer of the state

b. Chief pharmacist of government hospital

c. Assistant drug controller

d. All

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22. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of incurable diseases

c. Guidelines for clinical Trials

d. List of generic drugs

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23. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. UK

d. South Africa

24 / 50

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

a. 1985

b. 1955

c. 1940

d. 1950

25 / 50

25. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Enalapril

d. Metformin

26 / 50

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

a. Requirements of factory premises for the manufacturer of Homeopathy drugs

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

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

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

27 / 50

27. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule H

d. Schedule G

28 / 50

28. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule A

c. Schedule P

d. Schedule B

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29. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase III

d. Phase V

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30. 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 Y

b. Schedule O

c. Schedule M

d. Schedule F

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31. 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 I

c. Schedule J

d. Schedule H

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32. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

33 / 50

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

a. Yellow

b. Blue

c. Red

d. White

34 / 50

34. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Poisons Act

d. Dangerous Drug Act

35 / 50

35. 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

36 / 50

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

a. Symbol X given in red

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

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

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

37 / 50

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

a. Eight

b. Four

c. Five

d. Six

38 / 50

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

a. Ointment formulation

b. Skin cosmetic preparation

c. Parenteral preparation

d. Ophthalmic preparation

39 / 50

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

a. Toilet preparations

b. Ayurvedic drugs

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

40 / 50

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

a. The officer in charge of drugs control organization

b. President of India

c. Chief Administrator medical officer of state

d. Government Analyst

41 / 50

41. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Dangerous drugs Act

d. Spurious drugs Act

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

a. V

b. X

c. W

d. Y

44 / 50

44. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1954

d. 1948

45 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

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

d. A cool place

46 / 50

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

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule R

47 / 50

47. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. India

d. Zimbabwe

48 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. Area required to open wholesale drug store

49 / 50

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

a. Seven

b. Five

c. Nine

d. Six

50 / 50

50. Schedule J is related to

a. Pack sizes of drugs.

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

c. GMP

d. Curable disease

Your score is

The average score is 37%