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

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1 / 50

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

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

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

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

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

2 / 50

2. Dettol comes under

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule N

3 / 50

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

a. W

b. X

c. V

d. Y

4 / 50

4. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

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

d. Standard for cosmetics

5 / 50

5. 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

6 / 50

6. Pack size of drug is covered under

a. Schedule O

b. Schedule R

c. Schedule P1

d. Schedule P

7 / 50

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

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

8 / 50

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

a. Six

b. Five

c. Nine

d. Seven

9 / 50

9. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

10 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

11 / 50

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

12 / 50

12. In 1954 one of the following act is passed

a. Poisonous Act.

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Narcotic and psychotropic substance Act

13 / 50

13. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase II

d. Phase I

14 / 50

14. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

15 / 50

15. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Enalapril

d. Metformin

16 / 50

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

a. White

b. Blue

c. Red

d. Yellow

17 / 50

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

a. Chief Administrator medical officer of state

b. The officer in charge of drugs control organization

c. Government Analyst

d. President of India

18 / 50

18. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. Guidelines for clinical Trials

c. List of generic drugs

d. None of the above

19 / 50

19. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Insecticide Act

20 / 50

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

a. D

b. A

c. FF

d. Q

21 / 50

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

a. 1

b. 4

c. 3

d. 2

22 / 50

22. Patent Act is established in

a. 1940

b. 1970

c. 1919

d. 1948

23 / 50

23. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Denmark

d. Brazil

24 / 50

24. TGA is regulatory agency of………….

a. Denmark

b. India

c. Australia

d. Zimbabwe

25 / 50

25. 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. Misbranded Drug

d. Adulterated Drug

26 / 50

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

a. Schedule R

b. Schedule Q

c. Schedule P

d. Schedule O

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. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

29 / 50

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

a. 500 square meters

b. 150 square meters

c. 400 square meters

d. 250 square meters

30 / 50

30. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. B

d. X

31 / 50

31. 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

32 / 50

32. 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

33 / 50

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

a. Assistant drug controller

b. Chief administrative medical officer of the state

c. Chief pharmacist of government hospital

d. All

34 / 50

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

a. In cold place

b. At temperature which not exceed 5°C

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

d. At temperature which not exceed 20°C

35 / 50

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

a. Drug Controller

b. Central Government

c. President, Pharmacy Council of India

d. Ministry of Education

36 / 50

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

a. Eight

b. Six

c. Four

d. Five

37 / 50

37. Schedule J is related to

a. Pack sizes of drugs.

b. GMP

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

d. Curable disease

38 / 50

38. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

b. Determine Possible therapeutic uses, Effective doses range

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

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

39 / 50

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

a. 21

b. 20

c. 21B

d. 20B

40 / 50

40. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Homeopathy product

41 / 50

41. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

42 / 50

42. 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. Temperature not exceeding 5°C

d. A Cold place

43 / 50

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

a. Toilet preparations

b. Schedule ‘C’ ‘G’ drugs

c. Ayurvedic drugs

d. Misbranded drugs

44 / 50

44. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Banned drugs

d. Dangerous drugs Act

45 / 50

45. 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

46 / 50

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

a. 1950

b. 1940

c. 1955

d. 1985

47 / 50

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

a. R

b. R1

c. S

d. O

48 / 50

48. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

49 / 50

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

c. Symbol X given in red

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

50 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Parenteral preparation

Your score is

The average score is 38%