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 / 50

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

2 / 50

2. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1985

d. 1919

3 / 50

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

a. Temperature not exceeding 5°C

b. A cool place

c. A Cold place

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

4 / 50

4. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. A

d. X

5 / 50

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Ointment formulation

6 / 50

6. 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 F

b. Schedule O

c. Schedule Y

d. Schedule M

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7. 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

8 / 50

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

a. R1

b. S

c. R

d. O

9 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Misbranded drugs

d. Ayurvedic drugs

10 / 50

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

a. FF

b. D

c. A

d. Q

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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. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

13 / 50

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

a. 1985

b. 1950

c. 1940

d. 1955

14 / 50

14. 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. True Drug

d. Spurious Drug

15 / 50

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

a. Blue

b. Red

c. White

d. Yellow

16 / 50

16. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Denmark

d. Brazil

17 / 50

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

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

18 / 50

18. Schedule C is related to

a. List of Biological and Immunological product

b. List of Allopathic product

c. List of Ayurvedic product

d. List of Homeopathy product

19 / 50

19. Schedule J is related to

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

b. Pack sizes of drugs.

c. GMP

d. Curable disease

20 / 50

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

a. Five

b. Six

c. Nine

d. Seven

21 / 50

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

a. Chief administrative medical officer of the state

b. All

c. Assistant drug controller

d. Chief pharmacist of government hospital

22 / 50

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

a. Every 3 year

b. Every 5 year

c. Every 6 year

d. Every 2 year

23 / 50

23. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Poisonous Act.

24 / 50

24. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule H

d. Schedule J

25 / 50

25. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Brazil

d. Denmark

26 / 50

26. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule B

d. Schedule A

27 / 50

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

a. Central Government

b. President, Pharmacy Council of India

c. Drug Controller

d. Ministry of Education

28 / 50

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

a. The officer in charge of drugs control organization

b. Government Analyst

c. Chief Administrator medical officer of state

d. President of India

29 / 50

29. Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

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

d. List of minimum equipment for efficient running of pharmacy

30 / 50

30. 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. X

d. V

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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

32 / 50

32. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Dangerous Drug Act

c. Insecticide Act

d. Poisons Act

33 / 50

33. 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

34 / 50

34. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase V

d. Phase I

35 / 50

35. Patent Act is established in

a. 1919

b. 1940

c. 1948

d. 1970

36 / 50

36. Dettol comes under

a. Schedule Q

b. Schedule O

c. Schedule P

d. Schedule N

37 / 50

37. 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. Determine Possible therapeutic uses, Effective doses range

d. Long time adverse effects aster marketing drug

38 / 50

38. 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

39 / 50

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

a. 250 square meters

b. 400 square meters

c. 500 square meters

d. 150 square meters

40 / 50

40. 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

41 / 50

41. TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. Denmark

d. India

42 / 50

42. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

43 / 50

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

a. Four

b. Eight

c. Six

d. Five

44 / 50

44. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Spurious drugs Act

d. Over the counter drugs

45 / 50

45. Example of Schedule G drug is

a. Metformin

b. Cefuroxime

c. Enalapril

d. Barbital

46 / 50

46. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P1

d. Schedule P

47 / 50

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

a. 3

b. 1

c. 4

d. 2

48 / 50

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

a. At temperature which not exceed 5°C

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

c. In cold place

d. At temperature which not exceed 20°C

49 / 50

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

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

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

c. Symbol X given in red

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

50 / 50

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

a. 1-10 patients

b. 10-12 patients

c. 500 patients

d. 100 patients

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The average score is 37%