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

241

1 / 50

1. 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 Y

c. Schedule F

d. Schedule M

2 / 50

2. 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

3 / 50

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

a. A

b. FF

c. D

d. Q

4 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

5 / 50

5. Schedule J is related to

a. GMP

b. Pack sizes of drugs.

c. Curable disease

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

6 / 50

6. 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

7 / 50

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

a. Five

b. Six

c. Eight

d. Four

8 / 50

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

a. 1-10 patients

b. 10-12 patients

c. 500 patients

d. 100 patients

9 / 50

9. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Homeopathy product

10 / 50

10. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule J

d. Schedule K

11 / 50

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

a. Red

b. Blue

c. White

d. Yellow

12 / 50

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

a. UK

b. South Africa

c. Denmark

d. Brazil

13 / 50

13. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Narcotic and psychotropic substance Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

14 / 50

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

15 / 50

15. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1954

d. 1948

16 / 50

16. Dettol comes under

a. Schedule N

b. Schedule P

c. Schedule Q

d. Schedule O

17 / 50

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

a. 2

b. 1

c. 4

d. 3

18 / 50

18. 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. Chief Administrator medical officer of state

d. Government Analyst

19 / 50

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

a. In cold place

b. At temperature which not exceed 5°C

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

d. At temperature which not exceed 20°C

20 / 50

20. 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

21 / 50

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

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

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

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

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

22 / 50

22. 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 N displayed on left top corner of the label.

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

23 / 50

23. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Banned drugs

d. Spurious drugs Act

24 / 50

24. Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule P1

25 / 50

25. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

26 / 50

26. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

27 / 50

27. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

b. Determine Possible therapeutic uses, Effective doses range

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

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

28 / 50

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

a. Every 6 year

b. Every 2 year

c. Every 5 year

d. Every 3 year

29 / 50

29. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. India

d. Australia

30 / 50

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

a. Schedule O

b. Schedule P

c. Schedule R

d. Schedule Q

31 / 50

31. 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. X

d. W

32 / 50

32. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. Denmark

d. South Africa

33 / 50

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

a. 1940

b. 1950

c. 1955

d. 1985

34 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

35 / 50

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

a. R1

b. R

c. S

d. O

36 / 50

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

a. 21

b. 20B

c. 20

d. 21B

37 / 50

37. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Metformin

d. Barbital

38 / 50

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

a. G

b. K

c. H

d. X

39 / 50

39. 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

40 / 50

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

a. Nine

b. Five

c. Six

d. Seven

41 / 50

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

a. All

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. Assistant drug controller

42 / 50

42. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

43 / 50

43. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

44 / 50

44. 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. Spurious Drug

b. Misbranded Drug

c. Adulterated Drug

d. True Drug

45 / 50

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

a. President, Pharmacy Council of India

b. Central Government

c. Drug Controller

d. Ministry of Education

46 / 50

46. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

47 / 50

47. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase I

d. Phase II

48 / 50

48. Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule H

d. Schedule Y

49 / 50

49. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 26

d. Form 24

50 / 50

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

a. A Cold place

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

c. Temperature not exceeding 5°C

d. A cool place

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The average score is 35%