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. Patent Act is established in

a. 1948

b. 1919

c. 1940

d. 1970

2 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Misbranded drugs

3 / 50

3. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

4 / 50

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

a. 4

b. 1

c. 3

d. 2

5 / 50

5. 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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6. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

7 / 50

7. 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

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

a. 400 square meters

b. 250 square meters

c. 150 square meters

d. 500 square meters

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9. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 24

d. Form 26

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10. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Homeopathy product

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

a. G

b. X

c. K

d. H

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12. 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 M

b. Schedule F

c. Schedule Y

d. Schedule O

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13. Pack size of drug is covered under

a. Schedule O

b. Schedule R

c. Schedule P1

d. Schedule P

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

a. Schedule O

b. Schedule Q

c. Schedule R

d. Schedule P

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

a. Q

b. A

c. FF

d. D

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16. MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. UK

d. Brazil

17 / 50

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

a. Every 6 year

b. Every 2 year

c. Every 3 year

d. Every 5 year

18 / 50

18. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

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19. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of generic drugs

d. List of incurable diseases

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20. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

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21. 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

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22. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

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

d. Long time adverse effects aster marketing drug

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

a. List of minimum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

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24. 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 I

d. Schedule J

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

a. Nine

b. Five

c. Seven

d. Six

26 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

27 / 50

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

a. Blue

b. Red

c. Yellow

d. White

28 / 50

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

a. President, Pharmacy Council of India

b. Central Government

c. Drug Controller

d. Ministry of Education

29 / 50

29. Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule Q

d. Schedule A

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30. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule N

d. Schedule Q

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. All

32 / 50

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

a. 20

b. 21

c. 21B

d. 20B

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

a. Temperature not exceeding 5°C

b. A Cold place

c. A cool place

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

34 / 50

34. Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Barbital

d. Enalapril

35 / 50

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

a. List of prescription drugs

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. Requirements of factory premises

36 / 50

36. 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. In cold place

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

37 / 50

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

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

38 / 50

38. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Banned drugs

d. Over the counter drugs

39 / 50

39. 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. True Drug

c. Adulterated Drug

d. Misbranded Drug

40 / 50

40. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

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41. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

42 / 50

42. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule J

c. Schedule P

d. Schedule L

43 / 50

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

a. Six

b. Five

c. Eight

d. Four

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44. 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.

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45. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. Denmark

d. UK

46 / 50

46. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

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

a. Chief Administrator medical officer of state

b. President of India

c. The officer in charge of drugs control organization

d. Government Analyst

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48. Schedule J is related to

a. GMP

b. Curable disease

c. Pack sizes of drugs.

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

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

a. R1

b. R

c. O

d. S

50 / 50

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

a. 1940

b. 1950

c. 1985

d. 1955

Your score is

The average score is 37%