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. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase I

d. Phase III

2 / 50

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

a. Q

b. FF

c. A

d. D

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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. Spurious Drug

b. True Drug

c. Misbranded Drug

d. Adulterated Drug

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4. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. India

d. Australia

5 / 50

5. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule Q

d. Schedule P

6 / 50

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Ministry of Education

d. Central Government

7 / 50

7. 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 G

d. Schedule H

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

a. List of minimum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

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9. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. South Africa

d. Denmark

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

a. 1950

b. 1985

c. 1940

d. 1955

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11. 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 N displayed on left top corner of the label.

d. Symbol X given in red

12 / 50

12. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

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

a. 250 square meters

b. 400 square meters

c. 150 square meters

d. 500 square meters

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14. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Metformin

d. Cefuroxime

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

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule R

16 / 50

16. Patent Act is established in

a. 1948

b. 1940

c. 1919

d. 1970

17 / 50

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

a. Six

b. Four

c. Eight

d. Five

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18. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule O

d. Schedule P

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19. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

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21. 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 prescription drugs

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

d. Requirements of factory premises

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22. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule Y

d. Schedule G

23 / 50

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

a. O

b. R

c. R1

d. S

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

a. 21B

b. 20B

c. 21

d. 20

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25. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

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26. 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

27 / 50

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

a. In cold place

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. At temperature which not exceed 20°C

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28. 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. Chief administrative medical officer of the state

d. All

29 / 50

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

a. White

b. Red

c. Yellow

d. Blue

30 / 50

30. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

31 / 50

31. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

32 / 50

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

a. President of India

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. Government Analyst

33 / 50

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

a. 1-10 patients

b. 100 patients

c. 10-12 patients

d. 500 patients

34 / 50

34. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

35 / 50

35. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. List of incurable diseases

d. None of the above

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36. 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

37 / 50

37. 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

38 / 50

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

a. X

b. V

c. W

d. Y

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39. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

40 / 50

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

a. Seven

b. Five

c. Nine

d. Six

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41. Schedule J is related to

a. GMP

b. Curable disease

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

d. Pack sizes of drugs.

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42. 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

43 / 50

43. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. A

d. X

44 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

45 / 50

45. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

46 / 50

46. 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

47 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 3 year

d. Every 5 year

48 / 50

48. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Allopathic product

d. List of Biological and Immunological product

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49. Injection syringe and needles are covered under

a. Schedule P

b. Schedule A

c. Schedule Q

d. Schedule B

50 / 50

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

a. 3

b. 4

c. 2

d. 1

Your score is

The average score is 37%