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. Six

b. Eight

c. Four

d. Five

2 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

3 / 50

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

a. Chief pharmacist of government hospital

b. Assistant drug controller

c. Chief administrative medical officer of the state

d. All

4 / 50

4. 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. Government Analyst

d. President of India

5 / 50

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

a. H

b. G

c. X

d. K

6 / 50

6. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Poisons Act

d. Spurious Drug Act

7 / 50

7. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 27

d. Form 24

8 / 50

8. 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. In cold place

d. At temperature which not exceed 20°C

9 / 50

9. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

10 / 50

10. 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

11 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Central Government

d. Drug Controller

12 / 50

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

a. A

b. FF

c. Q

d. D

13 / 50

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

a. List of prescription drugs

b. Requirements of factory premises

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

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

14 / 50

14. 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 N displayed on left top corner of the label.

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

15 / 50

15. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule J

c. Schedule L

d. Schedule P

16 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Parenteral preparation

17 / 50

17. Schedule C is related to

a. List of Ayurvedic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Allopathic product

18 / 50

18. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Poisonous Act.

c. Drug and magic Remedies Act

d. Narcotic and psychotropic substance Act

19 / 50

19. TGA is regulatory agency of………….

a. Australia

b. India

c. Zimbabwe

d. Denmark

20 / 50

20. Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule P1

d. Schedule O

21 / 50

21. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Brazil

d. Denmark

22 / 50

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

a. 500 square meters

b. 400 square meters

c. 250 square meters

d. 150 square meters

23 / 50

23. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase II

d. Phase V

24 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

25 / 50

25. Biological and Biotechnological products are included in schedule.

a. B

b. C and C1

c. X

d. A

26 / 50

26. Schedule J is related to

a. Pack sizes of drugs.

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

c. GMP

d. Curable disease

27 / 50

27. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

28 / 50

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

a. 2

b. 3

c. 4

d. 1

29 / 50

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

a. Schedule O

b. Schedule R

c. Schedule Q

d. Schedule P

30 / 50

30. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Cefuroxime

d. Barbital

31 / 50

31. Hatch Waxman Act is related to

a. Over the counter drugs

b. Banned drugs

c. Spurious drugs Act

d. Dangerous drugs Act

32 / 50

32. 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. 20B

d. 20

33 / 50

33. 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. Misbranded Drug

c. Adulterated Drug

d. Spurious Drug

34 / 50

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

a. Schedule I

b. Schedule J

c. Schedule G

d. Schedule H

35 / 50

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

a. Seven

b. Nine

c. Five

d. Six

36 / 50

36. 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

37 / 50

37. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1919

d. 1954

38 / 50

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

a. Red

b. Blue

c. Yellow

d. White

39 / 50

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

a. Every 3 year

b. Every 2 year

c. Every 6 year

d. Every 5 year

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. V

b. X

c. W

d. Y

41 / 50

41. Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

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

42 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

43 / 50

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

a. A Cold place

b. A cool place

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

d. Temperature not exceeding 5°C

44 / 50

44. 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 F

c. Schedule M

d. Schedule Y

45 / 50

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

a. 1-10 patients

b. 10-12 patients

c. 500 patients

d. 100 patients

46 / 50

46. Patent Act is established in

a. 1940

b. 1948

c. 1919

d. 1970

47 / 50

47. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule N

48 / 50

48. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule H

d. Schedule G

49 / 50

49. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

50 / 50

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

a. R1

b. O

c. S

d. R

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The average score is 38%