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. Dettol comes under

a. Schedule P

b. Schedule Q

c. Schedule N

d. Schedule O

2 / 50

2. 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 manufacture of Medical device

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

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

3 / 50

3. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase III

d. Phase V

4 / 50

4. Schedule J is related to

a. GMP

b. Curable disease

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

d. Pack sizes of drugs.

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 F

b. Schedule Y

c. Schedule M

d. Schedule O

6 / 50

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

a. 500 square meters

b. 250 square meters

c. 400 square meters

d. 150 square meters

7 / 50

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

a. Requirements of factory premises

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

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

d. List of prescription drugs

8 / 50

8. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

9 / 50

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

a. Toilet preparations

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

10 / 50

10. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of incurable diseases

d. List of generic drugs

11 / 50

11. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Spurious drugs Act

d. Banned drugs

12 / 50

12. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 27

d. Form 25

13 / 50

13. Example of Schedule G drug is

a. Barbital

b. Metformin

c. Enalapril

d. Cefuroxime

14 / 50

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. The officer in charge of drugs control organization

d. President of India

15 / 50

15. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule K

d. Schedule P

16 / 50

16. 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.

17 / 50

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

a. Yellow

b. Blue

c. White

d. Red

18 / 50

18. 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

19 / 50

19. 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

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 temperature which not exceed 5°C

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

21 / 50

21. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. Australia

d. India

22 / 50

22. 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

23 / 50

23. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Homeopathy product

d. List of Biological and Immunological product

24 / 50

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

a. Eight

b. Four

c. Six

d. Five

25 / 50

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

a. South Africa

b. Brazil

c. UK

d. Denmark

26 / 50

26. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1985

d. 1948

27 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

28 / 50

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

a. 1940

b. 1955

c. 1985

d. 1950

29 / 50

29. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

c. Long time adverse effects aster marketing drug

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

30 / 50

30. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

31 / 50

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

a. Schedule I

b. Schedule H

c. Schedule J

d. Schedule G

32 / 50

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

a. FF

b. A

c. Q

d. D

33 / 50

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

a. A Cold place

b. Temperature not exceeding 5°C

c. A cool place

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

34 / 50

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

a. 3

b. 4

c. 1

d. 2

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. V

d. W

36 / 50

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

a. 20

b. 20B

c. 21

d. 21B

37 / 50

37. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

38 / 50

38. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

39 / 50

39. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule A

d. Schedule B

40 / 50

40. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. X

d. C and C1

41 / 50

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

a. Schedule Q

b. Schedule R

c. Schedule P

d. Schedule O

42 / 50

42. Pack size of drug is covered under

a. Schedule O

b. Schedule R

c. Schedule P

d. Schedule P1

43 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

44 / 50

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

a. Ophthalmic preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Parenteral preparation

45 / 50

45. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Insecticide Act

46 / 50

46. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

47 / 50

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

a. Ministry of Education

b. Central Government

c. President, Pharmacy Council of India

d. Drug Controller

48 / 50

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

a. Nine

b. Seven

c. Six

d. Five

49 / 50

49. 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. Spurious Drug

b. Misbranded Drug

c. True Drug

d. Adulterated Drug

50 / 50

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

a. O

b. R1

c. S

d. R

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The average score is 37%