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

360

1 / 50

1. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase V

d. Phase I

2 / 50

2. Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

c. GMP

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

3 / 50

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

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

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

c. Requirements of factory premises

d. List of prescription drugs

4 / 50

4. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 26

d. Form 24

5 / 50

5. 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. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

6 / 50

6. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule O

d. Schedule R

7 / 50

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

a. H

b. X

c. K

d. G

8 / 50

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

a. Every 2 year

b. Every 5 year

c. Every 6 year

d. Every 3 year

9 / 50

9. Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

10 / 50

10. 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

11 / 50

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

a. Schedule H

b. Schedule G

c. Schedule I

d. Schedule J

12 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

13 / 50

13. 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

14 / 50

14. 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 M

d. Schedule O

15 / 50

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

a. 100 patients

b. 1-10 patients

c. 10-12 patients

d. 500 patients

16 / 50

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

a. 250 square meters

b. 150 square meters

c. 400 square meters

d. 500 square meters

17 / 50

17. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Spurious Drug Act

d. Dangerous Drug Act

18 / 50

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

a. FF

b. D

c. Q

d. A

19 / 50

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

a. X

b. W

c. V

d. Y

20 / 50

20. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule P

c. Schedule L

d. Schedule J

21 / 50

21. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule P

d. Schedule O

22 / 50

22. Schedule C is related to

a. List of Biological and Immunological product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Allopathic product

23 / 50

23. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule P

d. Schedule A

24 / 50

24. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Over the counter drugs

d. Spurious drugs Act

25 / 50

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

a. O

b. R1

c. S

d. R

26 / 50

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

a. 1985

b. 1955

c. 1940

d. 1950

27 / 50

27. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Cefuroxime

d. Barbital

28 / 50

28. As per D and C act schedule T stated about

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

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

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

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

29 / 50

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

a. Five

b. Six

c. Four

d. Eight

30 / 50

30. TGA is regulatory agency of………….

a. India

b. Denmark

c. Australia

d. Zimbabwe

31 / 50

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

a. Chief administrative medical officer of the state

b. Assistant drug controller

c. All

d. Chief pharmacist of government hospital

32 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

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

d. A cool place

33 / 50

33. 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

34 / 50

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

a. 1

b. 4

c. 2

d. 3

35 / 50

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

a. Red

b. White

c. Blue

d. Yellow

36 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

37 / 50

37. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

38 / 50

38. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. A

d. C and C1

39 / 50

39. 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. True Drug

c. Misbranded Drug

d. Adulterated Drug

40 / 50

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

a. Five

b. Nine

c. Six

d. Seven

41 / 50

41. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1985

c. 1948

d. 1919

42 / 50

42. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

43 / 50

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

a. Symbol X given in red

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

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

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

44 / 50

44. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule G

d. Schedule Y

45 / 50

45. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Brazil

d. Denmark

46 / 50

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

a. Central Government

b. Ministry of Education

c. Drug Controller

d. President, Pharmacy Council of India

47 / 50

47. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of incurable diseases

c. Guidelines for clinical Trials

d. List of generic drugs

48 / 50

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

a. 21B

b. 21

c. 20

d. 20B

49 / 50

49. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Drug and magic Remedies Act

50 / 50

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

a. At temperature which not exceed 5°C

b. In cold place

c. At temperature which not exceed 20°C

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

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