Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test Noteskarts

Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test

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

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

a. Five

b. Nine

c. Six

d. Seven

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

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3. 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

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4. Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

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5. 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 F

b. Schedule M

c. Schedule O

d. Schedule Y

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

a. At temperature which not exceed 20°C

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. In cold place

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

a. 1940

b. 1985

c. 1950

d. 1955

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

a. 3

b. 4

c. 1

d. 2

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9. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. India

d. Australia

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

a. S

b. R

c. O

d. R1

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11. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

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

a. H

b. K

c. G

d. X

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

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Ayurvedic drugs

d. Toilet preparations

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14. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule Q

d. Schedule N

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15. 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

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

a. Every 2 year

b. Every 6 year

c. Every 5 year

d. Every 3 year

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

a. Chief Administrator medical officer of state

b. The officer in charge of drugs control organization

c. Government Analyst

d. President of India

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

a. 400 square meters

b. 500 square meters

c. 150 square meters

d. 250 square meters

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19. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

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20. 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

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21. 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

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

a. White

b. Red

c. Blue

d. Yellow

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23. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase V

d. Phase I

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

a. Drug Controller

b. Ministry of Education

c. Central Government

d. President, Pharmacy Council of India

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25. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

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

a. 20B

b. 21

c. 20

d. 21B

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27. 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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28. 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 Allopathy drugs

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

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29. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule J

c. Schedule P

d. Schedule K

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30. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

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31. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 25

d. Form 24

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

a. Four

b. Six

c. Eight

d. Five

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33. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. South Africa

d. Denmark

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

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

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

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

d. Symbol X given in red

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

a. Area for opening retail pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

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36. In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. The Medical Termination of pregnancy Act

d. Drug and magic Remedies Act

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

a. A cool place

b. A Cold place

c. Temperature not exceeding 5°C

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

38 / 50

38. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule P

d. Schedule A

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39. Schedule C is related to

a. List of Biological and Immunological product

b. List of Allopathic product

c. List of Homeopathy product

d. List of Ayurvedic product

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40. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule H

d. Schedule Y

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

a. All

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. Chief pharmacist of government hospital

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42. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Spurious Drug Act

d. Dangerous Drug Act

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43. 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

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44. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

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45. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Dangerous drugs Act

d. Banned drugs

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

a. Schedule P

b. Schedule Q

c. Schedule R

d. Schedule O

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47. Example of Schedule G drug is

a. Metformin

b. Cefuroxime

c. Enalapril

d. Barbital

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48. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. None of the above

d. Guidelines for clinical Trials

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

a. Q

b. D

c. FF

d. A

50 / 50

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

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

b. List of prescription drugs

c. Requirements of factory premises

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

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