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 X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of generic drugs

c. Guidelines for clinical Trials

d. List of incurable diseases

2 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

3 / 50

3. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

4 / 50

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

a. Eight

b. Five

c. Six

d. Four

5 / 50

5. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Denmark

d. Brazil

6 / 50

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

a. S

b. R1

c. R

d. O

7 / 50

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

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

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

c. Symbol X given in red

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

8 / 50

8. 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 Allopathy drugs

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

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

9 / 50

9. 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. Chief pharmacist of government hospital

d. Assistant drug controller

10 / 50

10. Hatch Waxman Act is related to

a. Over the counter drugs

b. Banned drugs

c. Spurious drugs Act

d. Dangerous drugs Act

11 / 50

11. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

12 / 50

12. Schedule J is related to

a. GMP

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

c. Pack sizes of drugs.

d. Curable disease

13 / 50

13. 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 F

b. Schedule Y

c. Schedule O

d. Schedule M

14 / 50

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

a. Nine

b. Five

c. Six

d. Seven

15 / 50

15. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

16 / 50

16. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. A

d. C and C1

17 / 50

17. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Poisons Act

d. Dangerous Drug Act

18 / 50

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

a. Red

b. Blue

c. Yellow

d. White

19 / 50

19. As per schedule P Carbenicillin Sodium Powder Should be Stored in/at

a. Temperature not exceeding 5°C

b. A cool place

c. Well closed container, protect from light, in cool place, protect from light

d. A Cold place

20 / 50

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

a. 10-12 patients

b. 100 patients

c. 1-10 patients

d. 500 patients

21 / 50

21. Pack size of drug is covered under

a. Schedule O

b. Schedule P1

c. Schedule R

d. Schedule P

22 / 50

22. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase I

d. Phase V

23 / 50

23. 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

24 / 50

24. Patent Act is established in

a. 1948

b. 1940

c. 1970

d. 1919

25 / 50

25. Schedule C is related to

a. List of Homeopathy product

b. List of Biological and Immunological product

c. List of Allopathic product

d. List of Ayurvedic product

26 / 50

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

a. The officer in charge of drugs control organization

b. Government Analyst

c. Chief Administrator medical officer of state

d. President of India

27 / 50

27. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

28 / 50

28. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Metformin

d. Enalapril

29 / 50

29. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

c. Determine Possible therapeutic uses, Effective doses range

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

30 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

31 / 50

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

a. FF

b. D

c. Q

d. A

32 / 50

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

a. H

b. X

c. K

d. G

33 / 50

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

a. 2

b. 4

c. 1

d. 3

34 / 50

34. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule N

35 / 50

35. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule K

d. Schedule J

36 / 50

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

a. 400 square meters

b. 150 square meters

c. 250 square meters

d. 500 square meters

37 / 50

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

a. At temperature which not exceed 5°C

b. In cold place

c. At temperature which not exceed 20°C

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

38 / 50

38. 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

39 / 50

39. 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. Spurious Drug

d. Misbranded Drug

40 / 50

40. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

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

41 / 50

41. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule A

c. Schedule B

d. Schedule P

42 / 50

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

a. 1985

b. 1955

c. 1950

d. 1940

43 / 50

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

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Ayurvedic drugs

44 / 50

44. 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. W

d. X

45 / 50

45. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1954

d. 1919

46 / 50

46. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule Y

d. Schedule G

47 / 50

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

a. Central Government

b. President, Pharmacy Council of India

c. Drug Controller

d. Ministry of Education

48 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule R

d. Schedule O

49 / 50

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

d. Requirements of factory premises

50 / 50

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

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The average score is 37%