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

358

1 / 50

1. 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)

2 / 50

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

a. S

b. O

c. R1

d. R

3 / 50

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

a. Central Government

b. Drug Controller

c. Ministry of Education

d. President, Pharmacy Council of India

4 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

5 / 50

5. TGA is regulatory agency of………….

a. Zimbabwe

b. India

c. Australia

d. Denmark

6 / 50

6. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. Narcotic and psychotropic substance Act

d. The Medical Termination of pregnancy Act

7 / 50

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

a. 21

b. 20B

c. 21B

d. 20

8 / 50

8. 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 G

c. Schedule H

d. Schedule I

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. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule J

c. Schedule K

d. Schedule P

11 / 50

11. Schedule C is related to

a. List of Biological and Immunological product

b. List of Ayurvedic product

c. List of Allopathic product

d. List of Homeopathy product

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. X

b. V

c. W

d. Y

13 / 50

13. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule O

d. Schedule Q

14 / 50

14. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase I

d. Phase III

15 / 50

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. President of India

d. Government Analyst

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

a. Requirements of factory premises

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

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

d. List of prescription drugs

18 / 50

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

a. FF

b. D

c. Q

d. A

19 / 50

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

a. Seven

b. Nine

c. Five

d. Six

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20. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. List of incurable diseases

d. None of the above

21 / 50

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

a. Four

b. Six

c. Eight

d. Five

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

a. 3

b. 4

c. 2

d. 1

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23. 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

24 / 50

24. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

25 / 50

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

a. UK

b. South Africa

c. Brazil

d. Denmark

26 / 50

26. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

27 / 50

27. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

28 / 50

28. Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule Q

d. Schedule B

29 / 50

29. Patent Act is established in

a. 1919

b. 1940

c. 1970

d. 1948

30 / 50

30. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

d. Standard for cosmetics

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31. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

32 / 50

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

33 / 50

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

a. White

b. Blue

c. Red

d. Yellow

34 / 50

34. MCC is regulatory agency of ……………

a. Brazil

b. Denmark

c. UK

d. South Africa

35 / 50

35. 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

36 / 50

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

a. 100 patients

b. 500 patients

c. 10-12 patients

d. 1-10 patients

37 / 50

37. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

38 / 50

38. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

39 / 50

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

a. All

b. Assistant drug controller

c. Chief administrative medical officer of the state

d. Chief pharmacist of government hospital

40 / 50

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

a. K

b. X

c. H

d. G

41 / 50

41. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule G

d. Schedule Y

42 / 50

42. 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

43 / 50

43. Schedule J is related to

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

b. Pack sizes of drugs.

c. Curable disease

d. GMP

44 / 50

44. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Banned drugs

c. Over the counter drugs

d. Dangerous drugs Act

45 / 50

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

a. Ointment formulation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Parenteral preparation

46 / 50

46. 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

47 / 50

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

a. Every 3 year

b. Every 2 year

c. Every 5 year

d. Every 6 year

48 / 50

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

a. At temperature which not exceed 5°C

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

c. At temperature which not exceed 20°C

d. In cold place

49 / 50

49. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

50 / 50

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

a. Symbol X given in red

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

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

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

Your score is

The average score is 37%