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

366

1 / 50

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

a. O

b. R

c. R1

d. S

2 / 50

2. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. Guidelines for clinical Trials

c. None of the above

d. List of generic drugs

3 / 50

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

a. 1950

b. 1955

c. 1985

d. 1940

4 / 50

4. Pack size of drug is covered under

a. Schedule O

b. Schedule P1

c. Schedule P

d. Schedule R

5 / 50

5. Schedule C is related to

a. List of Biological and Immunological product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Allopathic product

6 / 50

6. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Standard for cosmetics

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

d. Requirement of factory premises and hygienic condition to complied

7 / 50

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

a. Every 6 year

b. Every 5 year

c. Every 2 year

d. Every 3 year

8 / 50

8. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. B

d. X

9 / 50

9. 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 I

c. Schedule J

d. Schedule H

10 / 50

10. Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule B

d. Schedule P

11 / 50

11. 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

12 / 50

12. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule N

13 / 50

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

a. Six

b. Five

c. Nine

d. Seven

14 / 50

14. Schedule J is related to

a. Curable disease

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

c. GMP

d. Pack sizes of drugs.

15 / 50

15. 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. K

d. H

16 / 50

16. Insulin injection according to schedule P is should be stored

a. In cold place

b. At the Temperature 2°C to 8°C and it must not allow to freeze

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

17 / 50

17. 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

18 / 50

18. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 24

d. Form 25

19 / 50

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

a. Yellow

b. Red

c. Blue

d. White

20 / 50

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

a. Q

b. D

c. FF

d. A

21 / 50

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

a. Requirements of factory premises

b. List of prescription drugs

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

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

22 / 50

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

a. Six

b. Eight

c. Four

d. Five

23 / 50

23. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1954

d. 1985

24 / 50

24. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule H

d. Schedule J

25 / 50

25. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Cefuroxime

d. Barbital

26 / 50

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

a. Schedule Q

b. Schedule O

c. Schedule P

d. Schedule R

27 / 50

27. TGA is regulatory agency of………….

a. India

b. Denmark

c. Australia

d. Zimbabwe

28 / 50

28. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

29 / 50

29. Patent Act is established in

a. 1948

b. 1919

c. 1940

d. 1970

30 / 50

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

a. Assistant drug controller

b. All

c. Chief administrative medical officer of the state

d. Chief pharmacist of government hospital

31 / 50

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

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

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

c. Symbol X given in red

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

32 / 50

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

a. 150 square meters

b. 500 square meters

c. 250 square meters

d. 400 square meters

33 / 50

33. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule K

d. Schedule L

34 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Toilet preparations

d. Ayurvedic drugs

35 / 50

35. 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. Misbranded Drug

d. Spurious Drug

36 / 50

36. 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. A Cold place

d. Temperature not exceeding 5°C

37 / 50

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

a. President of India

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. Government Analyst

38 / 50

38. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Spurious drugs Act

d. Banned drugs

39 / 50

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

a. 100 patients

b. 10-12 patients

c. 1-10 patients

d. 500 patients

40 / 50

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

a. 4

b. 3

c. 2

d. 1

41 / 50

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

42 / 50

42. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Poisons Act

c. Insecticide Act

d. Spurious Drug Act

43 / 50

43. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

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 Y

b. Schedule F

c. Schedule O

d. Schedule M

45 / 50

45. 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

46 / 50

46. 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

47 / 50

47. 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. X

d. V

48 / 50

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

a. President, Pharmacy Council of India

b. Central Government

c. Drug Controller

d. Ministry of Education

49 / 50

49. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Denmark

d. Brazil

50 / 50

50. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

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The average score is 38%