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

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

a. 1

b. 2

c. 4

d. 3

2 / 50

2. 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

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3. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Denmark

d. Brazil

4 / 50

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

a. Every 6 year

b. Every 3 year

c. Every 5 year

d. Every 2 year

5 / 50

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. All

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6. MHRA is regulatory agency of ……….....

a. South Africa

b. Brazil

c. UK

d. Denmark

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7. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule Y

d. Schedule G

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8. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

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9. 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

10 / 50

10. 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. Government Analyst

d. Chief Administrator medical officer of state

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

a. Blue

b. White

c. Yellow

d. Red

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12. 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 Homeopathy drugs

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

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

13 / 50

13. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase V

d. Phase I

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14. Patent Act is established in

a. 1948

b. 1970

c. 1940

d. 1919

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15. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Cefuroxime

d. Barbital

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16. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule B

d. Schedule A

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

a. 500 square meters

b. 250 square meters

c. 400 square meters

d. 150 square meters

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18. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Drug and magic Remedies Act

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

a. Eight

b. Six

c. Four

d. Five

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

a. Temperature not exceeding 5°C

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

c. A cool place

d. A Cold place

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21. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 24

d. Form 25

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22. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. A

d. X

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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

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

a. S

b. R

c. O

d. R1

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25. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Spurious drugs Act

d. Dangerous drugs Act

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26. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1985

d. 1948

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

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

a. 10-12 patients

b. 500 patients

c. 100 patients

d. 1-10 patients

29 / 50

29. Schedule C is related to

a. List of Biological and Immunological product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Allopathic product

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

a. 20

b. 21B

c. 20B

d. 21

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31. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

32 / 50

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

a. In cold place

b. At temperature which not exceed 5°C

c. At temperature which not exceed 20°C

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

33 / 50

33. 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. Long time adverse effects aster marketing drug

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

34 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Drug Controller

d. Central Government

35 / 50

35. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

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36. Schedule J is related to

a. Curable disease

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

c. GMP

d. Pack sizes of drugs.

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37. 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 G

d. Schedule I

38 / 50

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

a. FF

b. A

c. Q

d. D

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

a. X

b. Y

c. W

d. V

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40. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of incurable diseases

c. List of generic drugs

d. None of the above

41 / 50

41. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

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

d. List of minimum equipment for efficient running of pharmacy

42 / 50

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

a. Misbranded drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

43 / 50

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

a. Schedule O

b. Schedule Q

c. Schedule R

d. Schedule P

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44. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule K

d. Schedule L

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

a. Seven

b. Five

c. Nine

d. Six

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46. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P1

d. Schedule P

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

a. List of maximum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

48 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Skin cosmetic preparation

d. Ointment formulation

49 / 50

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

a. 1950

b. 1940

c. 1955

d. 1985

50 / 50

50. 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. Spurious Drug

d. True Drug

Your score is

The average score is 37%