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

a. Government Analyst

b. President of India

c. Chief Administrator medical officer of state

d. The officer in charge of drugs control organization

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2. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule G

d. Schedule J

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

a. FF

b. D

c. Q

d. A

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4. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Poisons Act

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5. 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

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6. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. X

d. C and C1

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7. Schedule J is related to

a. GMP

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

c. Pack sizes of drugs.

d. Curable disease

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8. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

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9. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

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10. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. List of incurable diseases

d. None of the above

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11. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

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

a. 21

b. 20B

c. 21B

d. 20

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13. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule P

d. Schedule R

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

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

a. Four

b. Eight

c. Five

d. Six

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

a. Red

b. Blue

c. Yellow

d. White

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17. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase III

d. Phase V

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18. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1948

c. 1985

d. 1919

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19. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule J

d. Schedule K

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20. Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Barbital

d. Metformin

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21. 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. In cold place

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

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

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

b. Symbol N is red 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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23. The Education Regulation (ER) is published in official gazette by

a. President, Pharmacy Council of India

b. Ministry of Education

c. Drug Controller

d. Central Government

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24. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Spurious drugs Act

c. Banned drugs

d. Over the counter drugs

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

a. 100 patients

b. 10-12 patients

c. 500 patients

d. 1-10 patients

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

a. Schedule G

b. Schedule I

c. Schedule J

d. Schedule H

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

a. 1950

b. 1955

c. 1985

d. 1940

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

a. A Cold place

b. A cool place

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

d. Temperature not exceeding 5°C

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

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule Q

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31. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. South Africa

d. Denmark

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

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33. Patent Act is established in

a. 1940

b. 1970

c. 1919

d. 1948

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34. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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35. 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 Y

c. Schedule O

d. Schedule M

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

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37. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 24

d. Form 27

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38. 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 manufacture of Medical device

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

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

a. R

b. O

c. R1

d. S

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40. 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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41. Schedule N states

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

b. Standard for cosmetics

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

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42. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

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

a. Every 5 year

b. Every 3 year

c. Every 2 year

d. Every 6 year

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44. 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

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

a. 500 square meters

b. 400 square meters

c. 250 square meters

d. 150 square meters

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

a. K

b. X

c. H

d. G

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

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

a. Seven

b. Nine

c. Five

d. Six

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

a. 1

b. 3

c. 2

d. 4

50 / 50

50. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

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