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

351

1 / 50

1. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule A

d. Schedule P

2 / 50

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

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

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 manufacture of Medical device

3 / 50

3. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Banned drugs

d. Spurious drugs Act

4 / 50

4. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Cefuroxime

d. Metformin

5 / 50

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

a. Red

b. White

c. Yellow

d. Blue

6 / 50

6. 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

7 / 50

7. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Poisonous Act.

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

8 / 50

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

a. 500 square meters

b. 250 square meters

c. 150 square meters

d. 400 square meters

9 / 50

9. Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

10 / 50

10. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Spurious Drug Act

d. Poisons Act

11 / 50

11. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Standard for cosmetics

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

d. Requirement of factory premises and hygienic condition to complied

12 / 50

12. 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. True Drug

b. Adulterated Drug

c. Misbranded Drug

d. Spurious Drug

13 / 50

13. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. A

d. X

14 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

15 / 50

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

a. 1955

b. 1940

c. 1985

d. 1950

16 / 50

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

a. O

b. R

c. S

d. R1

17 / 50

17. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase II

d. Phase I

18 / 50

18. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. List of generic drugs

d. Guidelines for clinical Trials

19 / 50

19. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

20 / 50

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

d. Long time adverse effects aster marketing drug

21 / 50

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

a. Eight

b. Four

c. Five

d. Six

22 / 50

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

a. Schedule P

b. Schedule O

c. Schedule Q

d. Schedule R

23 / 50

23. MHRA is regulatory agency of ……….....

a. Brazil

b. South Africa

c. Denmark

d. UK

24 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

25 / 50

25. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

26 / 50

26. 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 X given in red

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

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

27 / 50

27. 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 F

c. Schedule M

d. Schedule O

28 / 50

28. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule K

d. Schedule L

29 / 50

29. TGA is regulatory agency of………….

a. Australia

b. Zimbabwe

c. Denmark

d. India

30 / 50

30. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule N

d. Schedule Q

31 / 50

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

a. Schedule J

b. Schedule H

c. Schedule I

d. Schedule G

32 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Parenteral preparation

33 / 50

33. 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

34 / 50

34. Schedule J is related to

a. Curable disease

b. GMP

c. Pack sizes of drugs.

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

35 / 50

35. 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

36 / 50

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

a. FF

b. D

c. Q

d. A

37 / 50

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. The officer in charge of drugs control organization

d. President of India

38 / 50

38. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

39 / 50

39. 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

40 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

c. A cool place

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

41 / 50

41. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1948

d. 1954

42 / 50

42. 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. G

d. H

43 / 50

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

a. 20B

b. 21B

c. 21

d. 20

44 / 50

44. 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

45 / 50

45. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule Y

d. Schedule G

46 / 50

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

a. 500 patients

b. 1-10 patients

c. 100 patients

d. 10-12 patients

47 / 50

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

a. W

b. Y

c. V

d. X

48 / 50

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

a. Six

b. Five

c. Nine

d. Seven

49 / 50

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

a. 3

b. 2

c. 4

d. 1

50 / 50

50. 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 5°C

d. At temperature which not exceed 20°C

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The average score is 37%