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. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule P1

d. Schedule O

2 / 50

2. 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

3 / 50

3. Schedule N states

a. Standard for cosmetics

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

c. List of minimum equipment for efficient running of pharmacy

d. Requirement of factory premises and hygienic condition to complied

4 / 50

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

a. 1

b. 2

c. 3

d. 4

5 / 50

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

6 / 50

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

a. Chief Administrator medical officer of state

b. President of India

c. The officer in charge of drugs control organization

d. Government Analyst

7 / 50

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

a. Brazil

b. Denmark

c. South Africa

d. UK

8 / 50

8. 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)

9 / 50

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

a. Ointment formulation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Parenteral preparation

10 / 50

10. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule Y

d. Schedule G

11 / 50

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

a. R

b. R1

c. O

d. S

12 / 50

12. 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 J

c. Schedule H

d. Schedule I

13 / 50

13. Schedule J is related to

a. GMP

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

c. Curable disease

d. Pack sizes of drugs.

14 / 50

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

a. Eight

b. Five

c. Six

d. Four

15 / 50

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

a. All

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. Assistant drug controller

16 / 50

16. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase V

d. Phase III

17 / 50

17. 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. Requirements of factory premises

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

18 / 50

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

a. At temperature which not exceed 5°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 20°C

19 / 50

19. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of incurable diseases

c. None of the above

d. List of generic drugs

20 / 50

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

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

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

c. Symbol X given in red

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

21 / 50

21. 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

22 / 50

22. 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

23 / 50

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

a. Y

b. V

c. X

d. W

24 / 50

24. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

25 / 50

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

a. K

b. G

c. H

d. X

26 / 50

26. 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

27 / 50

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

a. 1950

b. 1955

c. 1985

d. 1940

28 / 50

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

a. Red

b. Blue

c. White

d. Yellow

29 / 50

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

30 / 50

30. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

31 / 50

31. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

32 / 50

32. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1985

c. 1919

d. 1948

33 / 50

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

a. 21

b. 21B

c. 20

d. 20B

34 / 50

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

a. FF

b. A

c. D

d. Q

35 / 50

35. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

36 / 50

36. Patent Act is established in

a. 1948

b. 1919

c. 1970

d. 1940

37 / 50

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

a. Five

b. Six

c. Nine

d. Seven

38 / 50

38. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

39 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 5 year

d. Every 6 year

40 / 50

40. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule J

d. Schedule P

41 / 50

41. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

42 / 50

42. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

43 / 50

43. Schedule C is related to

a. List of Biological and Immunological product

b. List of Homeopathy product

c. List of Allopathic product

d. List of Ayurvedic product

44 / 50

44. Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Barbital

d. Metformin

45 / 50

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

a. Ayurvedic drugs

b. Toilet preparations

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

46 / 50

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

a. A cool place

b. A Cold place

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

d. Temperature not exceeding 5°C

47 / 50

47. 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 O

b. Schedule Y

c. Schedule M

d. Schedule F

48 / 50

48. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Spurious drugs Act

d. Over the counter drugs

49 / 50

49. 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 manufacturer of Allopathy drugs

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

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

50 / 50

50. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Dangerous Drug Act

d. Poisons Act

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