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

a. Assistant drug controller

b. All

c. Chief administrative medical officer of the state

d. Chief pharmacist of government hospital

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

a. Area for opening retail pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. List of minimum equipments for efficiently running pharmacy

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3. 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 F

c. Schedule Y

d. Schedule O

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4. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1985

d. 1954

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5. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Parenteral preparation

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

a. 4

b. 3

c. 1

d. 2

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8. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

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9. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

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10. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

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11. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Enalapril

d. Metformin

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12. Schedule J is related to

a. GMP

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

c. Curable disease

d. Pack sizes of drugs.

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

a. X

b. G

c. H

d. K

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

a. 1-10 patients

b. 500 patients

c. 100 patients

d. 10-12 patients

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

a. Four

b. Five

c. Eight

d. Six

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16. 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 H displayed on right top corner of the label.

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

d. Symbol X given in red

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17. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule O

d. Schedule P

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18. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

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19. 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 H

c. Schedule I

d. Schedule J

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20. Patent Act is established in

a. 1948

b. 1970

c. 1919

d. 1940

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21. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. Denmark

d. UK

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

a. Blue

b. White

c. Red

d. Yellow

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

a. D

b. FF

c. A

d. Q

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24. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. Drug and magic Remedies Act

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25. TGA is regulatory agency of………….

a. Australia

b. India

c. Zimbabwe

d. Denmark

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26. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule J

d. Schedule K

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27. Injection syringe and needles are covered under

a. Schedule B

b. Schedule Q

c. Schedule P

d. Schedule A

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28. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of generic drugs

d. List of incurable diseases

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

a. A cool place

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

c. A Cold place

d. Temperature not exceeding 5°C

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30. 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 manufacture of Medical device

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

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

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

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule R

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32. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Over the counter drugs

d. Banned drugs

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33. 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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34. Which of the following is prohibited to be imported?

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

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

a. Every 5 year

b. Every 2 year

c. Every 3 year

d. Every 6 year

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

a. 1940

b. 1955

c. 1950

d. 1985

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

a. 21B

b. 21

c. 20

d. 20B

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

a. Six

b. Nine

c. Five

d. Seven

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40. 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

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41. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

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42. 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

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43. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

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

a. Central Government

b. Ministry of Education

c. President, Pharmacy Council of India

d. Drug Controller

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45. 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

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46. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. B

d. X

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47. 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. Misbranded Drug

c. Adulterated Drug

d. True Drug

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48. Coca, opium and hemp come under:

a. Insecticide Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Poisons Act

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

a. S

b. O

c. R

d. R1

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50. 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. Requirements of factory premises

d. List of prescription drugs

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