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

358

1 / 50

1. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Biological and Immunological product

2 / 50

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

a. 2

b. 1

c. 4

d. 3

3 / 50

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

a. 20B

b. 21B

c. 20

d. 21

4 / 50

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

a. Ayurvedic drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

5 / 50

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

a. Drug Controller

b. Central Government

c. Ministry of Education

d. President, Pharmacy Council of India

6 / 50

6. 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

7 / 50

7. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Cefuroxime

d. Metformin

8 / 50

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

a. W

b. Y

c. V

d. X

9 / 50

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

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule Q

10 / 50

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

a. X

b. G

c. H

d. K

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 I

b. Schedule H

c. Schedule J

d. Schedule G

12 / 50

12. Schedule J is related to

a. GMP

b. Curable disease

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

d. Pack sizes of drugs.

13 / 50

13. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Poisons Act

d. Insecticide Act

14 / 50

14. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

15 / 50

15. 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

16 / 50

16. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase III

d. Phase II

17 / 50

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

a. Nine

b. Seven

c. Six

d. Five

18 / 50

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

a. Four

b. Six

c. Five

d. Eight

19 / 50

19. 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

20 / 50

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

a. Chief pharmacist of government hospital

b. All

c. Assistant drug controller

d. Chief administrative medical officer of the state

21 / 50

21. Injection syringe and needles are covered under

a. Schedule P

b. Schedule A

c. Schedule Q

d. Schedule B

22 / 50

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

a. 250 square meters

b. 400 square meters

c. 500 square meters

d. 150 square meters

23 / 50

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

d. Requirements of factory premises

24 / 50

24. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

25 / 50

25. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

26 / 50

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

a. White

b. Yellow

c. Blue

d. Red

27 / 50

27. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. List of generic drugs

c. None of the above

d. Guidelines for clinical Trials

28 / 50

28. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

29 / 50

29. 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

30 / 50

30. 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.

31 / 50

31. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1948

d. 1954

32 / 50

32. 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

33 / 50

33. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 26

d. Form 27

34 / 50

34. Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule P1

35 / 50

35. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

36 / 50

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

a. 1940

b. 1955

c. 1950

d. 1985

37 / 50

37. 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. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

38 / 50

38. TGA is regulatory agency of………….

a. Zimbabwe

b. Denmark

c. India

d. Australia

39 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 2 year

d. Every 3 year

40 / 50

40. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

41 / 50

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

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

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

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

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

42 / 50

42. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

43 / 50

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

a. R

b. R1

c. S

d. O

44 / 50

44. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

45 / 50

45. MCC is regulatory agency of ……………

a. Brazil

b. UK

c. Denmark

d. South Africa

46 / 50

46. 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. Spurious Drug

c. Adulterated Drug

d. Misbranded Drug

47 / 50

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

a. A

b. D

c. FF

d. Q

48 / 50

48. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. C and C1

d. A

49 / 50

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

a. Ointment formulation

b. Ophthalmic preparation

c. Skin cosmetic preparation

d. Parenteral preparation

50 / 50

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

a. 100 patients

b. 500 patients

c. 10-12 patients

d. 1-10 patients

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The average score is 37%