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

a. H

b. G

c. X

d. K

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 O

b. Schedule F

c. Schedule M

d. Schedule Y

3 / 50

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

a. 2

b. 3

c. 1

d. 4

4 / 50

4. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 27

d. Form 24

5 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. Area for opening retail pharmacy

6 / 50

6. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule B

d. Schedule A

7 / 50

7. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule N

d. Schedule Q

8 / 50

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

a. 1985

b. 1955

c. 1950

d. 1940

9 / 50

9. Patent Act is established in

a. 1970

b. 1919

c. 1948

d. 1940

10 / 50

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

11 / 50

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

a. Chief pharmacist of government hospital

b. Assistant drug controller

c. All

d. Chief administrative medical officer of the state

12 / 50

12. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. UK

d. South Africa

13 / 50

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

a. 20

b. 21

c. 21B

d. 20B

14 / 50

14. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Dangerous Drug Act

c. Poisons Act

d. Insecticide Act

15 / 50

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

a. White

b. Blue

c. Red

d. Yellow

16 / 50

16. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1919

d. 1954

17 / 50

17. Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

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

18 / 50

18. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase I

d. Phase III

19 / 50

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

a. FF

b. D

c. Q

d. A

20 / 50

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

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

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

c. List of prescription drugs

d. Requirements of factory premises

21 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

22 / 50

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

a. 250 square meters

b. 150 square meters

c. 400 square meters

d. 500 square meters

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 H

b. Schedule I

c. Schedule J

d. Schedule G

24 / 50

24. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

25 / 50

25. 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. Determine Possible therapeutic uses, Effective doses range

d. Long time adverse effects aster marketing drug

26 / 50

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

a. Eight

b. Five

c. Six

d. Four

27 / 50

27. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

28 / 50

28. 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 displayed on left top corner of the label.

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

29 / 50

29. 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 Homeopathy drugs

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

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

30 / 50

30. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule J

d. Schedule P

31 / 50

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

a. Toilet preparations

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

32 / 50

32. 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

33 / 50

33. Schedule J is related to

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

b. Curable disease

c. GMP

d. Pack sizes of drugs.

34 / 50

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. President of India

d. Chief Administrator medical officer of state

35 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Central Government

d. Drug Controller

36 / 50

36. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Banned drugs

d. Dangerous drugs Act

37 / 50

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

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

38 / 50

38. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

39 / 50

39. 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

40 / 50

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

a. In cold place

b. At temperature which not exceed 5°C

c. At temperature which not exceed 20°C

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

41 / 50

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

a. Five

b. Nine

c. Seven

d. Six

42 / 50

42. 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

43 / 50

43. Biological and Biotechnological products are included in schedule.

a. B

b. C and C1

c. X

d. A

44 / 50

44. 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

45 / 50

45. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Enalapril

d. Metformin

46 / 50

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

a. Schedule R

b. Schedule P

c. Schedule Q

d. Schedule O

47 / 50

47. TGA is regulatory agency of………….

a. Denmark

b. India

c. Australia

d. Zimbabwe

48 / 50

48. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule G

d. Schedule J

49 / 50

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

a. S

b. R

c. R1

d. O

50 / 50

50. 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.

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The average score is 37%