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

a. Yellow

b. Red

c. White

d. Blue

2 / 50

2. 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. Misbranded Drug

c. True Drug

d. Spurious Drug

3 / 50

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

a. Drug Controller

b. Ministry of Education

c. Central Government

d. President, Pharmacy Council of India

4 / 50

4. MHRA is regulatory agency of ……….....

a. Denmark

b. UK

c. Brazil

d. South Africa

5 / 50

5. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of incurable diseases

c. List of generic drugs

d. None of the above

6 / 50

6. 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

7 / 50

7. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

8 / 50

8. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

9 / 50

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

a. R1

b. R

c. S

d. O

10 / 50

10. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Metformin

d. Enalapril

11 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Ayurvedic drugs

d. Misbranded drugs

12 / 50

12. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. C and C1

d. X

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

a. Schedule Q

b. Schedule R

c. Schedule P

d. Schedule O

14 / 50

14. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule N

d. Schedule P

15 / 50

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

a. Schedule G

b. Schedule H

c. Schedule I

d. Schedule J

16 / 50

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

a. 10-12 patients

b. 500 patients

c. 100 patients

d. 1-10 patients

17 / 50

17. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

18 / 50

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

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

b. List of prescription drugs

c. Requirements of factory premises

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

19 / 50

19. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

20 / 50

20. 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

21 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 5 year

d. Every 3 year

22 / 50

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

a. 4

b. 1

c. 3

d. 2

23 / 50

23. Patent Act is established in

a. 1948

b. 1970

c. 1919

d. 1940

24 / 50

24. Schedule J is related to

a. GMP

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

c. Curable disease

d. Pack sizes of drugs.

25 / 50

25. 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. Y

d. V

26 / 50

26. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

27 / 50

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

a. 500 square meters

b. 400 square meters

c. 150 square meters

d. 250 square meters

28 / 50

28. 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 manufacturer of Allopathy drugs

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

29 / 50

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

a. Nine

b. Seven

c. Five

d. Six

30 / 50

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

a. A

b. FF

c. D

d. Q

31 / 50

31. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Homeopathy product

d. List of Biological and Immunological product

32 / 50

32. Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule Q

d. Schedule B

33 / 50

33. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

b. Determine Possible therapeutic uses, Effective doses range

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

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

34 / 50

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

35 / 50

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

a. 20B

b. 20

c. 21B

d. 21

36 / 50

36. 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.

37 / 50

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

a. 1955

b. 1985

c. 1940

d. 1950

38 / 50

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

a. Six

b. Eight

c. Five

d. Four

39 / 50

39. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 27

d. Form 25

40 / 50

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

a. Chief pharmacist of government hospital

b. All

c. Chief administrative medical officer of the state

d. Assistant drug controller

41 / 50

41. Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule G

d. Schedule H

42 / 50

42. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase III

d. Phase I

43 / 50

43. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Poisonous Act.

c. Narcotic and psychotropic substance Act

d. Drug and magic Remedies Act

44 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

45 / 50

45. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

46 / 50

46. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule P

d. Schedule L

47 / 50

47. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Spurious drugs Act

d. Dangerous drugs Act

48 / 50

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

a. X

b. K

c. H

d. G

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

a. Chief Administrator medical officer of state

b. President of India

c. Government Analyst

d. The officer in charge of drugs control organization

50 / 50

50. 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 F

d. Schedule O

Your score is

The average score is 38%