Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law And Ethics DPEE Noteskarts

Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law and Ethics DPEE

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

Top 50 Question for Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law and Ethics DPEE

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

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

b. Symbol X given in red

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

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

2 / 50

2. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

3 / 50

3. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

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

a. 3

b. 1

c. 2

d. 4

5 / 50

5. 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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6. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule N

d. Schedule O

7 / 50

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

a. Blue

b. Yellow

c. White

d. Red

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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. List of maximum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. Area required to open wholesale drug store

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9. 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. True Drug

c. Spurious Drug

d. Adulterated Drug

10 / 50

10. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule J

d. Schedule K

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11. TGA is regulatory agency of………….

a. Denmark

b. India

c. Australia

d. Zimbabwe

12 / 50

12. Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

c. GMP

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

13 / 50

13. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

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

a. 150 square meters

b. 250 square meters

c. 400 square meters

d. 500 square meters

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

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

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

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

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

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16. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Banned drugs

d. Over the counter drugs

17 / 50

17. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase II

c. Phase I

d. Phase III

18 / 50

18. Patent Act is established in

a. 1940

b. 1919

c. 1948

d. 1970

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

a. A cool place

b. A Cold place

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

d. Temperature not exceeding 5°C

20 / 50

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

a. In cold place

b. At temperature which not exceed 20°C

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

d. At temperature which not exceed 5°C

21 / 50

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 drug exempted from the provision of import of drugs

c. List of prescription drugs

d. Requirements of factory premises

22 / 50

22. Schedule C is related to

a. List of Homeopathy product

b. List of Biological and Immunological product

c. List of Allopathic product

d. List of Ayurvedic product

23 / 50

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

a. FF

b. D

c. A

d. Q

24 / 50

24. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. All

26 / 50

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

a. Every 3 year

b. Every 2 year

c. Every 5 year

d. Every 6 year

27 / 50

27. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P1

d. Schedule P

28 / 50

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

a. Four

b. Eight

c. Five

d. Six

29 / 50

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

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Ayurvedic drugs

30 / 50

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

a. 21

b. 21B

c. 20B

d. 20

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

a. Nine

b. Five

c. Six

d. Seven

32 / 50

32. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1985

d. 1948

33 / 50

33. List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule H

b. Schedule J

c. Schedule G

d. Schedule I

34 / 50

34. Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule H

d. Schedule G

35 / 50

35. 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. W

d. V

36 / 50

36. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Enalapril

d. Metformin

37 / 50

37. 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

38 / 50

38. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 27

d. Form 24

39 / 50

39. 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

40 / 50

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

a. 1940

b. 1955

c. 1985

d. 1950

41 / 50

41. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. South Africa

d. UK

42 / 50

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

a. President of India

b. Government Analyst

c. Chief Administrator medical officer of state

d. The officer in charge of drugs control organization

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43. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. X

d. B

44 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Skin cosmetic preparation

45 / 50

45. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

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

d. Standard for cosmetics

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46. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Denmark

d. Brazil

47 / 50

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

a. 500 patients

b. 100 patients

c. 10-12 patients

d. 1-10 patients

48 / 50

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

a. Drug Controller

b. Central Government

c. Ministry of Education

d. President, Pharmacy Council of India

49 / 50

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

a. O

b. R1

c. S

d. R

50 / 50

50. 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

Your score is

The average score is 31%