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

345

1 / 50

1. Patent Act is established in

a. 1948

b. 1940

c. 1970

d. 1919

2 / 50

2. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase I

c. Phase II

d. Phase V

3 / 50

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

a. 21

b. 21B

c. 20B

d. 20

4 / 50

4. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 24

d. Form 26

5 / 50

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

a. Temperature not exceeding 5°C

b. A cool place

c. A Cold place

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

6 / 50

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

a. Symbol X given in red

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

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

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

7 / 50

7. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

8 / 50

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

a. Drug Controller

b. Central Government

c. Ministry of Education

d. President, Pharmacy Council of India

9 / 50

9. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

10 / 50

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

a. 1940

b. 1950

c. 1985

d. 1955

11 / 50

11. Biological and Biotechnological products are included in schedule.

a. X

b. A

c. C and C1

d. B

12 / 50

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

a. 100 patients

b. 500 patients

c. 1-10 patients

d. 10-12 patients

13 / 50

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

a. Six

b. Eight

c. Five

d. Four

14 / 50

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

a. D

b. Q

c. A

d. FF

15 / 50

15. 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. X

d. H

16 / 50

16. 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

17 / 50

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

a. V

b. X

c. Y

d. W

18 / 50

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

a. Blue

b. Yellow

c. White

d. Red

19 / 50

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

20 / 50

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

a. Ointment formulation

b. Parenteral preparation

c. Ophthalmic preparation

d. Skin cosmetic preparation

21 / 50

21. 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

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22. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule O

d. Schedule P

23 / 50

23. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

24 / 50

24. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Denmark

d. Brazil

25 / 50

25. 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. True Drug

c. Adulterated Drug

d. Misbranded Drug

26 / 50

26. 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

27 / 50

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

a. R1

b. R

c. O

d. S

28 / 50

28. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. South Africa

d. UK

29 / 50

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

a. The officer in charge of drugs control organization

b. Government Analyst

c. President of India

d. Chief Administrator medical officer of state

30 / 50

30. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. India

d. Zimbabwe

31 / 50

31. 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

32 / 50

32. 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 I

c. Schedule G

d. Schedule J

33 / 50

33. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

34 / 50

34. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

35 / 50

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

a. Schedule O

b. Schedule R

c. Schedule P

d. Schedule Q

36 / 50

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

a. Seven

b. Nine

c. Five

d. Six

37 / 50

37. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule H

d. Schedule J

38 / 50

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

a. 3

b. 2

c. 1

d. 4

39 / 50

39. 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

40 / 50

40. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Enalapril

d. Metformin

41 / 50

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

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

42 / 50

42. Schedule J is related to

a. Pack sizes of drugs.

b. Curable disease

c. GMP

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

43 / 50

43. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule Q

d. Schedule O

44 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 3 year

d. Every 5 year

45 / 50

45. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of incurable diseases

d. List of generic drugs

46 / 50

46. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Dangerous drugs Act

d. Banned drugs

47 / 50

47. 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. Chief pharmacist of government hospital

d. All

48 / 50

48. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Insecticide Act

d. Dangerous Drug Act

49 / 50

49. 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 drug exempted from the provision of import of drugs

c. List of prescription drugs

d. Requirements of factory premises

50 / 50

50. Schedule C is related to

a. List of Ayurvedic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Allopathic product

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