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

345

1 / 50

1. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule B

d. Schedule A

2 / 50

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

a. V

b. Y

c. X

d. W

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

a. Chief administrative medical officer of the state

b. All

c. Assistant drug controller

d. Chief pharmacist of government hospital

4 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

5 / 50

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

a. Five

b. Nine

c. Seven

d. Six

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6. 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

7 / 50

7. TGA is regulatory agency of………….

a. Denmark

b. India

c. Australia

d. Zimbabwe

8 / 50

8. Patent Act is established in

a. 1919

b. 1970

c. 1948

d. 1940

9 / 50

9. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase I

d. Phase V

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10. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule J

d. Schedule K

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11. Hatch Waxman Act is related to

a. Over the counter drugs

b. Banned drugs

c. Spurious drugs Act

d. Dangerous drugs Act

12 / 50

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

a. K

b. H

c. X

d. G

13 / 50

13. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Spurious Drug Act

d. Dangerous Drug Act

14 / 50

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

a. Six

b. Eight

c. Four

d. Five

15 / 50

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

a. S

b. O

c. R

d. R1

16 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Misbranded drugs

d. Ayurvedic drugs

17 / 50

17. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1948

d. 1954

18 / 50

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

a. 1950

b. 1955

c. 1985

d. 1940

19 / 50

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

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

b. Requirements of factory premises

c. List of prescription drugs

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

20 / 50

20. Example of Schedule G drug is

a. Barbital

b. Metformin

c. Enalapril

d. Cefuroxime

21 / 50

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

22 / 50

22. 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 Cold place

c. A cool place

d. Temperature not exceeding 5°C

23 / 50

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. Spurious Drug

c. True Drug

d. Adulterated Drug

24 / 50

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

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

b. Symbol X given in red

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

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

25 / 50

25. 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

26 / 50

26. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule R

d. Schedule O

27 / 50

27. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

28 / 50

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. President of India

29 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule O

d. Schedule R

30 / 50

30. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule J

d. Schedule H

31 / 50

31. 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.

32 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. Area for opening retail pharmacy

d. List of maximum equipments for efficiently running pharmacy

33 / 50

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

a. 500 square meters

b. 250 square meters

c. 150 square meters

d. 400 square meters

34 / 50

34. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule N

35 / 50

35. Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

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

d. Requirement of factory premises and hygienic condition to complied

36 / 50

36. 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

37 / 50

37. 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 H

c. Schedule J

d. Schedule G

38 / 50

38. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of incurable diseases

c. List of generic drugs

d. Guidelines for clinical Trials

39 / 50

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

a. 3

b. 4

c. 1

d. 2

40 / 50

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

a. Q

b. D

c. A

d. FF

41 / 50

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

a. White

b. Yellow

c. Blue

d. Red

42 / 50

42. 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

43 / 50

43. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

44 / 50

44. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

45 / 50

45. 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 Allopathy drugs

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

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

46 / 50

46. 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

47 / 50

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

a. 20

b. 21

c. 20B

d. 21B

48 / 50

48. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

49 / 50

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

d. Long time adverse effects aster marketing drug

50 / 50

50. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. South Africa

d. Denmark

Your score is

The average score is 37%