Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test Noteskarts

Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test

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

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1 / 50

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

a. Four

b. Eight

c. Six

d. Five

2 / 50

2. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

3 / 50

3. TGA is regulatory agency of………….

a. India

b. Australia

c. Denmark

d. Zimbabwe

4 / 50

4. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule N

d. Schedule O

5 / 50

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

a. Schedule P

b. Schedule Q

c. Schedule R

d. Schedule O

6 / 50

6. Schedule J is related to

a. Curable disease

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

c. Pack sizes of drugs.

d. GMP

7 / 50

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

a. 400 square meters

b. 150 square meters

c. 250 square meters

d. 500 square meters

8 / 50

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

a. 1985

b. 1955

c. 1950

d. 1940

9 / 50

9. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

10 / 50

10. 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 is red displayed on left top corner of the label

c. Symbol X given in red

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

11 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

12 / 50

12. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Allopathic product

d. List of Biological and Immunological product

13 / 50

13. 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 J

d. Schedule I

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 M

c. Schedule O

d. Schedule F

15 / 50

15. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

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

a. President of India

b. Government Analyst

c. Chief Administrator medical officer of state

d. The officer in charge of drugs control organization

17 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 6 year

d. Every 2 year

18 / 50

18. MHRA is regulatory agency of ……….....

a. UK

b. Denmark

c. Brazil

d. South Africa

19 / 50

19. 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 Ayurveda, Sidhha and Unani drugs

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

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

20 / 50

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Central Government

d. Ministry of Education

21 / 50

21. 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. True Drug

b. Adulterated Drug

c. Spurious Drug

d. Misbranded Drug

22 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Ayurvedic drugs

d. Toilet preparations

23 / 50

23. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

24 / 50

24. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Metformin

d. Cefuroxime

25 / 50

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

a. D

b. A

c. FF

d. Q

26 / 50

26. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1919

d. 1948

27 / 50

27. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Over the counter drugs

d. Banned drugs

28 / 50

28. Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule A

d. Schedule Q

29 / 50

29. 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. G

d. H

30 / 50

30. 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. 21

d. 20

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

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

b. A cool place

c. Temperature not exceeding 5°C

d. A Cold place

32 / 50

32. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

33 / 50

33. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule R

d. Schedule P1

34 / 50

34. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

35 / 50

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

a. 100 patients

b. 10-12 patients

c. 500 patients

d. 1-10 patients

36 / 50

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. All

d. Chief administrative medical officer of the state

37 / 50

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

a. Six

b. Five

c. Nine

d. Seven

38 / 50

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

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. List of minimum equipments for efficiently running pharmacy

39 / 50

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

a. R

b. R1

c. S

d. O

40 / 50

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

a. X

b. Y

c. W

d. V

41 / 50

41. 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

42 / 50

42. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

43 / 50

43. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

44 / 50

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

a. Red

b. Yellow

c. White

d. Blue

45 / 50

45. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

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

d. List of minimum equipment for efficient running of pharmacy

46 / 50

46. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule P

c. Schedule J

d. Schedule L

47 / 50

47. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase II

d. Phase I

48 / 50

48. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of generic drugs

d. List of incurable diseases

49 / 50

49. 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. In cold place

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

50 / 50

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

a. 2

b. 1

c. 4

d. 3

Your score is

The average score is 36%