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. Injection syringe and needles are covered under

a. Schedule P

b. Schedule B

c. Schedule Q

d. Schedule A

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2. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

3 / 50

3. MHRA is regulatory agency of ……….....

a. Denmark

b. UK

c. South Africa

d. Brazil

4 / 50

4. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

5 / 50

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

a. H

b. G

c. X

d. K

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

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule Q

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7. 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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8. Patent Act is established in

a. 1948

b. 1940

c. 1919

d. 1970

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

a. Every 2 year

b. Every 5 year

c. Every 3 year

d. Every 6 year

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10. 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. Misbranded Drug

b. Adulterated Drug

c. Spurious Drug

d. True Drug

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

a. Blue

b. White

c. Red

d. Yellow

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

a. Symbol H displayed on right 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 N displayed on left top corner of the label.

13 / 50

13. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

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14. 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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15. 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

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

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

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

c. List of prescription drugs

d. Requirements of factory premises

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17. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 27

d. Form 24

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

a. 1950

b. 1955

c. 1940

d. 1985

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

a. Seven

b. Six

c. Nine

d. Five

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

a. 10-12 patients

b. 1-10 patients

c. 500 patients

d. 100 patients

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21. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. List of generic drugs

c. None of the above

d. Guidelines for clinical Trials

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

a. A cool place

b. A Cold place

c. Temperature not exceeding 5°C

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

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

a. 250 square meters

b. 500 square meters

c. 150 square meters

d. 400 square meters

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

a. R

b. O

c. R1

d. S

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

a. Drug Controller

b. President, Pharmacy Council of India

c. Central Government

d. Ministry of Education

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26. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Spurious drugs Act

c. Banned drugs

d. Over the counter drugs

27 / 50

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

a. 2

b. 4

c. 3

d. 1

28 / 50

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

a. Ointment formulation

b. Skin cosmetic preparation

c. Parenteral preparation

d. Ophthalmic preparation

30 / 50

30. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. Drug and magic Remedies Act

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31. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

32 / 50

32. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. X

d. B

33 / 50

33. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule Y

d. Schedule G

34 / 50

34. 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 G

c. Schedule H

d. Schedule I

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

a. Chief pharmacist of government hospital

b. All

c. Assistant drug controller

d. Chief administrative medical officer of the state

37 / 50

37. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

38 / 50

38. TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. Denmark

d. India

39 / 50

39. 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

40 / 50

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

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Ayurvedic drugs

d. Toilet preparations

41 / 50

41. Dettol comes under

a. Schedule N

b. Schedule P

c. Schedule O

d. Schedule Q

42 / 50

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

a. At temperature which not exceed 20°C

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

c. At temperature which not exceed 5°C

d. In cold place

43 / 50

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

a. FF

b. D

c. Q

d. A

44 / 50

44. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1954

d. 1948

45 / 50

45. Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Barbital

d. Enalapril

46 / 50

46. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase I

c. Phase II

d. Phase V

47 / 50

47. 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 O

c. Schedule F

d. Schedule Y

48 / 50

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

a. Five

b. Six

c. Eight

d. Four

49 / 50

49. 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. 20B

d. 21B

50 / 50

50. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P1

d. Schedule P

Your score is

The average score is 38%