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

359

1 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 6 year

d. Every 2 year

2 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Parenteral preparation

3 / 50

3. 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 Y

b. Schedule F

c. Schedule O

d. Schedule M

4 / 50

4. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1954

d. 1948

5 / 50

5. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

6 / 50

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

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

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

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

7 / 50

7. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. South Africa

d. UK

8 / 50

8. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase III

d. Phase V

9 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

10 / 50

10. 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

11 / 50

11. 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

12 / 50

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

a. 21

b. 20

c. 20B

d. 21B

13 / 50

13. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule N

d. Schedule Q

14 / 50

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

a. Assistant drug controller

b. Chief administrative medical officer of the state

c. All

d. Chief pharmacist of government hospital

15 / 50

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

a. X

b. Y

c. W

d. V

16 / 50

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

a. Four

b. Eight

c. Five

d. Six

17 / 50

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

a. 3

b. 2

c. 1

d. 4

18 / 50

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

19 / 50

19. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

b. Determine Possible therapeutic uses, Effective doses range

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)

20 / 50

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

a. Yellow

b. White

c. Red

d. Blue

21 / 50

21. 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

22 / 50

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

a. 1950

b. 1940

c. 1985

d. 1955

23 / 50

23. Coca, opium and hemp come under:

a. Insecticide Act

b. Spurious Drug Act

c. Poisons Act

d. Dangerous Drug Act

24 / 50

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

a. X

b. K

c. H

d. G

25 / 50

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

a. S

b. O

c. R

d. R1

26 / 50

26. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule Y

d. Schedule G

27 / 50

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

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

b. Temperature not exceeding 5°C

c. A Cold place

d. A cool place

28 / 50

28. Patent Act is established in

a. 1919

b. 1940

c. 1948

d. 1970

29 / 50

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

a. Q

b. D

c. FF

d. A

30 / 50

30. 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

31 / 50

31. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule O

d. Schedule P

32 / 50

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

a. 500 patients

b. 10-12 patients

c. 100 patients

d. 1-10 patients

33 / 50

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

a. President, Pharmacy Council of India

b. Central Government

c. Drug Controller

d. Ministry of Education

34 / 50

34. Schedule J is related to

a. Pack sizes of drugs.

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

c. GMP

d. Curable disease

35 / 50

35. TGA is regulatory agency of………….

a. Australia

b. Zimbabwe

c. India

d. Denmark

36 / 50

36. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 24

d. Form 25

37 / 50

37. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. Denmark

d. UK

38 / 50

38. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

39 / 50

39. 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

40 / 50

40. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Allopathic product

41 / 50

41. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule B

d. Schedule A

42 / 50

42. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

43 / 50

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

a. Five

b. Six

c. Seven

d. Nine

44 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule R

d. Schedule O

45 / 50

45. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule K

d. Schedule L

46 / 50

46. 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. True Drug

b. Misbranded Drug

c. Adulterated Drug

d. Spurious Drug

47 / 50

47. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. List of incurable diseases

d. None of the above

48 / 50

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

49 / 50

49. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Metformin

d. Enalapril

50 / 50

50. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Dangerous drugs Act

d. Banned drugs

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The average score is 37%