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

a. Symbol X given in red

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

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

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

2 / 50

2. 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 M

b. Schedule O

c. Schedule F

d. Schedule Y

3 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. Area for opening retail pharmacy

4 / 50

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

a. Ointment formulation

b. Parenteral preparation

c. Ophthalmic preparation

d. Skin cosmetic preparation

5 / 50

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

a. Drug Controller

b. President, Pharmacy Council of India

c. Central Government

d. Ministry of Education

6 / 50

6. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

7 / 50

7. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

8 / 50

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

a. R1

b. R

c. S

d. O

9 / 50

9. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. Poisonous Act.

10 / 50

10. Schedule J is related to

a. GMP

b. Curable disease

c. Pack sizes of drugs.

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

11 / 50

11. MCC is regulatory agency of ……………

a. Denmark

b. South Africa

c. Brazil

d. UK

12 / 50

12. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule Q

d. Schedule P

13 / 50

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

a. 500 patients

b. 100 patients

c. 1-10 patients

d. 10-12 patients

14 / 50

14. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 26

d. Form 24

15 / 50

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

a. Five

b. Six

c. Nine

d. Seven

16 / 50

16. 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

17 / 50

17. 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. At temperature which not exceed 20°C

d. In cold place

18 / 50

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

a. Four

b. Eight

c. Five

d. Six

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

a. K

b. X

c. G

d. H

20 / 50

20. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule N

d. Schedule Q

21 / 50

21. Schedule C is related to

a. List of Biological and Immunological product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Allopathic product

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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. Temperature not exceeding 5°C

c. A cool place

d. A Cold place

23 / 50

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

a. Toilet preparations

b. Misbranded drugs

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

24 / 50

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

a. 1940

b. 1985

c. 1955

d. 1950

25 / 50

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

a. 250 square meters

b. 400 square meters

c. 150 square meters

d. 500 square meters

26 / 50

26. TGA is regulatory agency of………….

a. India

b. Australia

c. Denmark

d. Zimbabwe

27 / 50

27. 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 J

c. Schedule I

d. Schedule H

28 / 50

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

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

b. List of prescription drugs

c. Requirements of factory premises

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

29 / 50

29. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. None of the above

d. List of incurable diseases

30 / 50

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

a. A

b. D

c. Q

d. FF

31 / 50

31. Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Barbital

d. Enalapril

32 / 50

32. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

33 / 50

33. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule O

d. Schedule P

34 / 50

34. 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. True Drug

c. Misbranded Drug

d. Spurious Drug

35 / 50

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

a. Red

b. Yellow

c. Blue

d. White

36 / 50

36. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

37 / 50

37. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. X

d. B

38 / 50

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

a. 20

b. 21B

c. 21

d. 20B

39 / 50

39. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Poisons Act

d. Spurious Drug Act

40 / 50

40. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Banned drugs

d. Spurious drugs Act

41 / 50

41. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule J

c. Schedule P

d. Schedule K

42 / 50

42. 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

43 / 50

43. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Brazil

d. Denmark

44 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 3 year

d. Every 5 year

45 / 50

45. 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

46 / 50

46. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

47 / 50

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

a. 4

b. 3

c. 1

d. 2

48 / 50

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

a. V

b. X

c. W

d. Y

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49. 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 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 manufacture of Medical device

50 / 50

50. 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. Government Analyst

d. Chief Administrator medical officer of state

Your score is

The average score is 37%