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

a. Eight

b. Five

c. Four

d. Six

2 / 50

2. Schedule J is related to

a. GMP

b. Curable disease

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

d. Pack sizes of drugs.

3 / 50

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

a. Yellow

b. White

c. Red

d. Blue

4 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

5 / 50

5. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. X

d. C and C1

6 / 50

6. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule Q

d. Schedule P

7 / 50

7. Patent Act is established in

a. 1970

b. 1940

c. 1919

d. 1948

8 / 50

8. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1985

d. 1954

9 / 50

9. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule J

d. Schedule G

10 / 50

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

a. President of India

b. Chief Administrator medical officer of state

c. Government Analyst

d. The officer in charge of drugs control organization

11 / 50

11. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. Guidelines for clinical Trials

d. None of the above

12 / 50

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

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

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 X given in red

13 / 50

13. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Metformin

d. Enalapril

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. Adulterated Drug

b. Misbranded Drug

c. True Drug

d. Spurious Drug

15 / 50

15. 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. Chief administrative medical officer of the state

d. All

16 / 50

16. 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

17 / 50

17. 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 Y

d. Schedule M

18 / 50

18. MCC is regulatory agency of ……………

a. Brazil

b. UK

c. South Africa

d. Denmark

19 / 50

19. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

20 / 50

20. 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 Allopathy drugs

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

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

21 / 50

21. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

22 / 50

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

a. Schedule O

b. Schedule R

c. Schedule Q

d. Schedule P

23 / 50

23. 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. In cold place

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

24 / 50

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

a. 1-10 patients

b. 500 patients

c. 10-12 patients

d. 100 patients

25 / 50

25. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

26 / 50

26. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

27 / 50

27. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

d. Standard for cosmetics

28 / 50

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

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Ayurvedic drugs

29 / 50

29. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

30 / 50

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

a. 1940

b. 1955

c. 1985

d. 1950

31 / 50

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

a. Parenteral preparation

b. Ophthalmic preparation

c. Ointment formulation

d. Skin cosmetic preparation

32 / 50

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

a. Q

b. D

c. A

d. FF

33 / 50

33. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 25

d. Form 24

34 / 50

34. 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. List of prescription drugs

c. Requirements of factory premises

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

35 / 50

35. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Ayurvedic product

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

d. A Cold place

37 / 50

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

a. 2

b. 1

c. 3

d. 4

38 / 50

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

a. Central Government

b. President, Pharmacy Council of India

c. Drug Controller

d. Ministry of Education

39 / 50

39. Pack size of drug is covered under

a. Schedule O

b. Schedule P1

c. Schedule P

d. Schedule R

40 / 50

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

a. Y

b. V

c. X

d. W

41 / 50

41. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Dangerous drugs Act

d. Banned drugs

42 / 50

42. 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

43 / 50

43. MHRA is regulatory agency of ……….....

a. Brazil

b. UK

c. Denmark

d. South Africa

44 / 50

44. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

45 / 50

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

a. Every 3 year

b. Every 5 year

c. Every 6 year

d. Every 2 year

46 / 50

46. 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

47 / 50

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

a. Six

b. Nine

c. Five

d. Seven

48 / 50

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

a. R1

b. R

c. S

d. O

49 / 50

49. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule N

d. Schedule P

50 / 50

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

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The average score is 37%