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. Dettol comes under

a. Schedule Q

b. Schedule O

c. Schedule P

d. Schedule N

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 Y

d. Schedule F

3 / 50

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

a. At temperature which not exceed 20°C

b. In cold place

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

d. At temperature which not exceed 5°C

4 / 50

4. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

5 / 50

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

a. A

b. Q

c. FF

d. D

6 / 50

6. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

7 / 50

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

a. 1955

b. 1950

c. 1940

d. 1985

8 / 50

8. 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

9 / 50

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

a. 3

b. 2

c. 1

d. 4

10 / 50

10. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

c. Long time adverse effects aster marketing drug

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

11 / 50

11. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. List of minimum equipment for efficient running of pharmacy

d. Standard for cosmetics

12 / 50

12. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1948

d. 1954

13 / 50

13. In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. The Medical Termination of pregnancy Act

d. Drug and magic Remedies Act

14 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

15 / 50

15. Patent Act is established in

a. 1970

b. 1940

c. 1948

d. 1919

16 / 50

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

a. Seven

b. Five

c. Nine

d. Six

17 / 50

17. 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

18 / 50

18. MHRA is regulatory agency of ……….....

a. South Africa

b. Brazil

c. Denmark

d. UK

19 / 50

19. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule O

d. Schedule P

20 / 50

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

a. K

b. H

c. G

d. X

21 / 50

21. 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

22 / 50

22. Schedule J is related to

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

b. Pack sizes of drugs.

c. Curable disease

d. GMP

23 / 50

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

a. Ministry of Education

b. Central Government

c. President, Pharmacy Council of India

d. Drug Controller

24 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 2 year

d. Every 6 year

25 / 50

25. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of generic drugs

c. List of incurable diseases

d. Guidelines for clinical Trials

26 / 50

26. 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. Spurious Drug

c. Misbranded Drug

d. True Drug

27 / 50

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

a. Temperature not exceeding 5°C

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

c. A Cold place

d. A cool place

28 / 50

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

a. Requirements of factory premises

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

c. List of prescription drugs

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

29 / 50

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

a. Yellow

b. Red

c. Blue

d. White

30 / 50

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

a. 400 square meters

b. 250 square meters

c. 500 square meters

d. 150 square meters

31 / 50

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

a. Six

b. Five

c. Four

d. Eight

32 / 50

32. TGA is regulatory agency of………….

a. India

b. Denmark

c. Zimbabwe

d. Australia

33 / 50

33. Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule Q

d. Schedule B

34 / 50

34. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase III

d. Phase V

35 / 50

35. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule H

d. Schedule Y

36 / 50

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

a. Chief administrative medical officer of the state

b. Assistant drug controller

c. Chief pharmacist of government hospital

d. All

37 / 50

37. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

38 / 50

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

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule R

39 / 50

39. 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.

40 / 50

40. Schedule C is related to

a. List of Biological and Immunological product

b. List of Homeopathy product

c. List of Allopathic product

d. List of Ayurvedic product

41 / 50

41. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. Denmark

d. UK

42 / 50

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

a. 1-10 patients

b. 100 patients

c. 500 patients

d. 10-12 patients

43 / 50

43. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Banned drugs

d. Over the counter drugs

44 / 50

44. 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. 20B

d. 21B

45 / 50

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

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

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

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

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

46 / 50

46. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 27

c. Form 25

d. Form 26

47 / 50

47. Example of Schedule G drug is

a. Metformin

b. Cefuroxime

c. Barbital

d. Enalapril

48 / 50

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

a. Parenteral preparation

b. Ophthalmic preparation

c. Skin cosmetic preparation

d. Ointment formulation

49 / 50

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

a. O

b. S

c. R

d. R1

50 / 50

50. 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 J

c. Schedule I

d. Schedule G

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The average score is 37%