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

367

1 / 50

1. Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule G

d. Schedule H

2 / 50

2. 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

3 / 50

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

a. 3

b. 4

c. 2

d. 1

4 / 50

4. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

5 / 50

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

a. Drug Controller

b. Ministry of Education

c. President, Pharmacy Council of India

d. Central Government

6 / 50

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

a. Assistant drug controller

b. Chief administrative medical officer of the state

c. All

d. Chief pharmacist of government hospital

7 / 50

7. Schedule J is related to

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

b. Curable disease

c. Pack sizes of drugs.

d. GMP

8 / 50

8. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 24

d. Form 27

9 / 50

9. 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

10 / 50

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

a. Seven

b. Five

c. Nine

d. Six

11 / 50

11. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

12 / 50

12. 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

13 / 50

13. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of generic drugs

d. List of incurable diseases

14 / 50

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

a. Ayurvedic drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

15 / 50

15. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

16 / 50

16. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

17 / 50

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

a. R

b. O

c. S

d. R1

18 / 50

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

a. At temperature which not exceed 20°C

b. In cold place

c. At temperature which not exceed 5°C

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

19 / 50

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

a. Yellow

b. White

c. Blue

d. Red

20 / 50

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

a. V

b. W

c. Y

d. X

21 / 50

21. Patent Act is established in

a. 1919

b. 1940

c. 1970

d. 1948

22 / 50

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

a. 1950

b. 1955

c. 1985

d. 1940

23 / 50

23. 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 Y

c. Schedule O

d. Schedule F

24 / 50

24. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Insecticide Act

d. Spurious Drug Act

25 / 50

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

26 / 50

26. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

c. List of minimum equipment for efficient running of pharmacy

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

27 / 50

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

a. Six

b. Eight

c. Four

d. Five

28 / 50

28. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule J

c. Schedule P

d. Schedule L

29 / 50

29. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule P

d. Schedule A

30 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

31 / 50

31. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

32 / 50

32. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

33 / 50

33. 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 maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

34 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Parenteral preparation

35 / 50

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

a. 500 square meters

b. 150 square meters

c. 400 square meters

d. 250 square meters

36 / 50

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

a. A cool place

b. Temperature not exceeding 5°C

c. A Cold place

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

37 / 50

37. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule P

d. Schedule O

38 / 50

38. List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule I

b. Schedule J

c. Schedule G

d. Schedule H

39 / 50

39. 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

40 / 50

40. 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

41 / 50

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

a. 21B

b. 20B

c. 20

d. 21

42 / 50

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

a. Symbol X given in red

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

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

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

43 / 50

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

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule Q

44 / 50

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

a. D

b. A

c. Q

d. FF

45 / 50

45. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1948

c. 1919

d. 1954

46 / 50

46. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Enalapril

d. Metformin

47 / 50

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

a. X

b. H

c. G

d. K

48 / 50

48. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Banned drugs

d. Spurious drugs Act

49 / 50

49. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

50 / 50

50. MHRA is regulatory agency of ……….....

a. Brazil

b. UK

c. Denmark

d. South Africa

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The average score is 38%