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 6 year

c. Every 2 year

d. Every 3 year

2 / 50

2. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule O

d. Schedule P

3 / 50

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

a. Blue

b. White

c. Yellow

d. Red

4 / 50

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

a. 100 patients

b. 10-12 patients

c. 1-10 patients

d. 500 patients

5 / 50

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

a. At temperature which not exceed 20°C

b. In cold place

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

d. At temperature which not exceed 5°C

6 / 50

6. 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

7 / 50

7. 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 M

c. Schedule O

d. Schedule F

8 / 50

8. 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 X given in red

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

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

9 / 50

9. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1919

d. 1948

10 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

11 / 50

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

a. Six

b. Four

c. Eight

d. Five

12 / 50

12. 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. V

d. W

13 / 50

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

a. 500 square meters

b. 250 square meters

c. 150 square meters

d. 400 square meters

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. Misbranded Drug

b. True Drug

c. Adulterated Drug

d. Spurious Drug

15 / 50

15. MCC is regulatory agency of ……………

a. Denmark

b. South Africa

c. UK

d. Brazil

16 / 50

16. 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 H

c. Schedule G

d. Schedule I

17 / 50

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

a. Q

b. D

c. A

d. FF

18 / 50

18. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. C and C1

d. X

19 / 50

19. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. Poisonous Act.

20 / 50

20. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 26

d. Form 24

21 / 50

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

a. Seven

b. Five

c. Six

d. Nine

22 / 50

22. Patent Act is established in

a. 1919

b. 1948

c. 1940

d. 1970

23 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Parenteral preparation

24 / 50

24. 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

25 / 50

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

a. 3

b. 1

c. 2

d. 4

26 / 50

26. 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

27 / 50

27. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

28 / 50

28. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Brazil

d. Denmark

29 / 50

29. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Dangerous Drug Act

c. Poisons Act

d. Insecticide Act

30 / 50

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

a. Ministry of Education

b. Drug Controller

c. Central Government

d. President, Pharmacy Council of India

31 / 50

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

a. 20B

b. 21

c. 20

d. 21B

32 / 50

32. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule P

d. Schedule K

33 / 50

33. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. Guidelines for clinical Trials

d. None of the above

34 / 50

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

a. 1955

b. 1940

c. 1950

d. 1985

35 / 50

35. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule Y

d. Schedule G

36 / 50

36. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

37 / 50

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

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule Q

38 / 50

38. 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

39 / 50

39. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

40 / 50

40. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

41 / 50

41. Schedule J is related to

a. Pack sizes of drugs.

b. GMP

c. Curable disease

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

42 / 50

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

a. O

b. R

c. S

d. R1

43 / 50

43. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Cefuroxime

d. Metformin

44 / 50

44. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

45 / 50

45. Injection syringe and needles are covered under

a. Schedule P

b. Schedule B

c. Schedule A

d. Schedule Q

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. X

c. K

d. H

47 / 50

47. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Spurious drugs Act

d. Banned drugs

48 / 50

48. 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 manufacture of Medical device

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

49 / 50

49. 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. Area for opening retail pharmacy

d. List of minimum equipments for efficiently running pharmacy

50 / 50

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. President of India

d. Chief Administrator medical officer of state

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The average score is 37%