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. 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. Chief pharmacist of government hospital

d. Assistant drug controller

2 / 50

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

a. 2

b. 3

c. 4

d. 1

3 / 50

3. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. Denmark

d. UK

4 / 50

4. 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. Spurious Drug

c. Adulterated Drug

d. True Drug

5 / 50

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

a. 500 patients

b. 10-12 patients

c. 1-10 patients

d. 100 patients

6 / 50

6. 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 J

d. Schedule I

7 / 50

7. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

8 / 50

8. 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 manufacture of Medical device

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

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

9 / 50

9. Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule P

d. Schedule B

10 / 50

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

a. R

b. R1

c. O

d. S

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

a. Every 2 year

b. Every 3 year

c. Every 5 year

d. Every 6 year

12 / 50

12. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule P

d. Schedule O

13 / 50

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

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

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

c. List of prescription drugs

d. Requirements of factory premises

14 / 50

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

a. Five

b. Eight

c. Four

d. Six

15 / 50

15. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

16 / 50

16. Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule Y

d. Schedule H

17 / 50

17. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

18 / 50

18. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase III

d. Phase II

19 / 50

19. 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

20 / 50

20. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1954

c. 1985

d. 1948

21 / 50

21. Schedule J is related to

a. Curable disease

b. GMP

c. Pack sizes of drugs.

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

22 / 50

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

a. A Cold place

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

c. A cool place

d. Temperature not exceeding 5°C

23 / 50

23. 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

24 / 50

24. 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

25 / 50

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

a. 21B

b. 21

c. 20B

d. 20

26 / 50

26. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

27 / 50

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

a. Schedule R

b. Schedule P

c. Schedule Q

d. Schedule O

28 / 50

28. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. C and C1

d. X

29 / 50

29. 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

30 / 50

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

a. D

b. Q

c. FF

d. A

31 / 50

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

a. 1985

b. 1940

c. 1955

d. 1950

32 / 50

32. 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. Area for opening retail pharmacy

d. List of maximum equipments for efficiently running pharmacy

33 / 50

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

a. Symbol X given in red

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

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

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

34 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Parenteral preparation

35 / 50

35. Patent Act is established in

a. 1919

b. 1970

c. 1940

d. 1948

36 / 50

36. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule N

37 / 50

37. 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

38 / 50

38. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Cefuroxime

d. Barbital

39 / 50

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

a. 250 square meters

b. 150 square meters

c. 400 square meters

d. 500 square meters

40 / 50

40. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. India

d. Zimbabwe

41 / 50

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

a. Nine

b. Six

c. Seven

d. Five

42 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Drug Controller

d. Central Government

43 / 50

43. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule J

d. Schedule K

44 / 50

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

a. White

b. Red

c. Yellow

d. Blue

45 / 50

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

a. W

b. X

c. Y

d. V

46 / 50

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

a. G

b. K

c. H

d. X

47 / 50

47. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 26

d. Form 27

48 / 50

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

a. Toilet preparations

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

49 / 50

49. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Dangerous drugs Act

d. Over the counter drugs

50 / 50

50. In 1954 one of the following act is passed

a. Poisonous Act.

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Narcotic and psychotropic substance Act

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The average score is 37%