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

a. 21B

b. 20B

c. 20

d. 21

2 / 50

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

a. W

b. V

c. X

d. Y

3 / 50

3. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

4 / 50

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

a. X

b. G

c. H

d. K

5 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

6 / 50

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

7 / 50

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

a. Denmark

b. South Africa

c. Brazil

d. UK

8 / 50

8. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule K

d. Schedule J

9 / 50

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

a. Area for opening retail pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

10 / 50

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

a. Skin cosmetic preparation

b. Ophthalmic preparation

c. Ointment formulation

d. Parenteral preparation

11 / 50

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

a. 4

b. 2

c. 1

d. 3

12 / 50

12. 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

13 / 50

13. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule A

d. Schedule P

14 / 50

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

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

b. At temperature which not exceed 5°C

c. In cold place

d. At temperature which not exceed 20°C

15 / 50

15. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Poisonous Act.

c. The Medical Termination of pregnancy Act

d. Drug and magic Remedies Act

16 / 50

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

a. Schedule O

b. Schedule R

c. Schedule P

d. Schedule Q

17 / 50

17. 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. Spurious Drug

c. Misbranded Drug

d. True Drug

18 / 50

18. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

19 / 50

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

a. Government Analyst

b. President of India

c. The officer in charge of drugs control organization

d. Chief Administrator medical officer of state

20 / 50

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

a. R1

b. S

c. O

d. R

21 / 50

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

a. Five

b. Six

c. Eight

d. Four

22 / 50

22. 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

23 / 50

23. TGA is regulatory agency of………….

a. Denmark

b. India

c. Zimbabwe

d. Australia

24 / 50

24. 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

25 / 50

25. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule J

d. Schedule H

26 / 50

26. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase V

d. Phase I

27 / 50

27. 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 O

c. Schedule M

d. Schedule Y

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28. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. List of minimum equipment for efficient running of pharmacy

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

d. Standard for cosmetics

29 / 50

29. 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

30 / 50

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

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

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

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

d. Symbol X given in red

31 / 50

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

a. 500 patients

b. 100 patients

c. 1-10 patients

d. 10-12 patients

32 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 6 year

d. Every 2 year

33 / 50

33. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Dangerous drugs Act

d. Banned drugs

34 / 50

34. Schedule J is related to

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

b. Pack sizes of drugs.

c. GMP

d. Curable disease

35 / 50

35. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Barbital

d. Metformin

36 / 50

36. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

37 / 50

37. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. None of the above

d. List of incurable diseases

38 / 50

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

a. Red

b. Blue

c. Yellow

d. White

39 / 50

39. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1919

d. 1948

40 / 50

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

a. A Cold place

b. Temperature not exceeding 5°C

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

d. A cool place

41 / 50

41. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. B

d. A

42 / 50

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

a. Q

b. FF

c. D

d. A

43 / 50

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

44 / 50

44. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

45 / 50

45. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule Q

d. Schedule P

46 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

47 / 50

47. Patent Act is established in

a. 1940

b. 1919

c. 1970

d. 1948

48 / 50

48. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

c. Determine Possible therapeutic uses, Effective doses range

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

49 / 50

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

a. Nine

b. Five

c. Seven

d. Six

50 / 50

50. 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

Your score is

The average score is 37%