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. Patent Act is established in

a. 1919

b. 1970

c. 1948

d. 1940

2 / 50

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

a. Eight

b. Five

c. Four

d. Six

3 / 50

3. Schedule J is related to

a. Pack sizes of drugs.

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

c. Curable disease

d. GMP

4 / 50

4. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

5 / 50

5. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule B

d. Schedule A

6 / 50

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

a. Schedule O

b. Schedule Q

c. Schedule R

d. Schedule P

7 / 50

7. Schedule C is related to

a. List of Ayurvedic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Allopathic product

8 / 50

8. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase II

d. Phase V

9 / 50

9. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Barbital

d. Metformin

10 / 50

10. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1985

d. 1954

11 / 50

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

a. 1940

b. 1955

c. 1985

d. 1950

12 / 50

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

a. Requirements of factory premises

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

c. List of prescription drugs

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

13 / 50

13. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule L

d. Schedule K

14 / 50

14. 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. Misbranded Drug

b. Adulterated Drug

c. True Drug

d. Spurious Drug

15 / 50

15. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

16 / 50

16. 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 O

c. Schedule F

d. Schedule M

17 / 50

17. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Spurious drugs Act

d. Dangerous drugs Act

18 / 50

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

a. Red

b. White

c. Yellow

d. Blue

19 / 50

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

a. Area for opening retail pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. List of minimum equipments for efficiently running pharmacy

20 / 50

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

a. Nine

b. Seven

c. Five

d. Six

21 / 50

21. MHRA is regulatory agency of ……….....

a. UK

b. Denmark

c. Brazil

d. South Africa

22 / 50

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

a. Central Government

b. Drug Controller

c. President, Pharmacy Council of India

d. Ministry of Education

23 / 50

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

a. Y

b. W

c. X

d. V

24 / 50

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

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

b. At temperature which not exceed 20°C

c. In cold place

d. At temperature which not exceed 5°C

25 / 50

25. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. List of incurable diseases

d. Guidelines for clinical Trials

26 / 50

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. All

27 / 50

27. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule Q

d. Schedule N

28 / 50

28. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 24

d. Form 25

29 / 50

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

a. X

b. K

c. H

d. G

30 / 50

30. Schedule N states

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

b. Standard for cosmetics

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

31 / 50

31. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule J

d. Schedule H

32 / 50

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

a. 20B

b. 20

c. 21

d. 21B

33 / 50

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

34 / 50

34. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

35 / 50

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

a. 3

b. 4

c. 1

d. 2

36 / 50

36. 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

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. Government Analyst

d. Chief Administrator medical officer of state

38 / 50

38. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule O

d. Schedule R

39 / 50

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

a. A cool place

b. A Cold place

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

d. Temperature not exceeding 5°C

40 / 50

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

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

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

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

d. Symbol X given in red

41 / 50

41. 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 H

d. Schedule J

42 / 50

42. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

43 / 50

43. 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

44 / 50

44. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

c. Determine Possible therapeutic uses, Effective doses range

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

45 / 50

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

a. 100 patients

b. 10-12 patients

c. 500 patients

d. 1-10 patients

46 / 50

46. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. South Africa

d. Denmark

47 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

48 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Toilet preparations

d. Ayurvedic drugs

49 / 50

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

a. A

b. FF

c. D

d. Q

50 / 50

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

a. O

b. S

c. R1

d. R

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The average score is 37%