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. Pack size of drug is covered under

a. Schedule P

b. Schedule O

c. Schedule P1

d. Schedule R

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2. In 1954 one of the following act is passed

a. Poisonous Act.

b. Drug and magic Remedies Act

c. Narcotic and psychotropic substance Act

d. The Medical Termination of pregnancy Act

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3. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Banned drugs

d. Spurious drugs Act

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4. 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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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 Y

c. Schedule O

d. Schedule M

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6. 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. True Drug

c. Spurious Drug

d. Misbranded Drug

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

a. Chief pharmacist of government hospital

b. Assistant drug controller

c. All

d. Chief administrative medical officer of the state

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8. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule Q

d. Schedule O

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

a. Every 2 year

b. Every 3 year

c. Every 5 year

d. Every 6 year

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

a. Misbranded drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

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

a. Symbol X given in red

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

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

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

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12. Schedule J is related to

a. Pack sizes of drugs.

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

c. Curable disease

d. GMP

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13. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

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

a. K

b. G

c. X

d. H

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

a. Four

b. Five

c. Six

d. Eight

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16. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Poisons Act

d. Insecticide Act

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17. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule P

d. Schedule L

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18. Schedule C is related to

a. List of Ayurvedic product

b. List of Biological and Immunological product

c. List of Allopathic product

d. List of Homeopathy product

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19. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

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

a. Nine

b. Five

c. Seven

d. Six

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

a. Parenteral preparation

b. Ophthalmic preparation

c. Skin cosmetic preparation

d. Ointment formulation

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

a. Q

b. FF

c. A

d. D

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24. Aspirin sodium comes under

a. Schedule H

b. Schedule G

c. Schedule Y

d. Schedule J

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

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

b. Temperature not exceeding 5°C

c. A Cold place

d. A cool place

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26. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1954

d. 1948

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

a. 500 patients

b. 100 patients

c. 1-10 patients

d. 10-12 patients

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28. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 27

d. Form 24

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

a. 21

b. 20

c. 20B

d. 21B

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

a. R

b. S

c. O

d. R1

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31. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

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

a. Schedule O

b. Schedule R

c. Schedule Q

d. Schedule P

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

a. 1985

b. 1940

c. 1955

d. 1950

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34. Injection syringe and needles are covered under

a. Schedule P

b. Schedule A

c. Schedule B

d. Schedule Q

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35. 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 Homeopathy drugs

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

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

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

a. 2

b. 4

c. 3

d. 1

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

a. 400 square meters

b. 250 square meters

c. 500 square meters

d. 150 square meters

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38. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. South Africa

d. Denmark

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. President of India

d. Government Analyst

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40. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. UK

d. Brazil

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

a. Central Government

b. Drug Controller

c. President, Pharmacy Council of India

d. Ministry of Education

42 / 50

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

a. White

b. Yellow

c. Blue

d. Red

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

a. At temperature which not exceed 5°C

b. At temperature which not exceed 20°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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44. As per D and C Act “Schedule N” is related with

a. List of maximum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. Area for opening retail pharmacy

d. List of minimum equipments for efficiently running pharmacy

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45. TGA is regulatory agency of………….

a. Zimbabwe

b. Denmark

c. India

d. Australia

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

a. Y

b. V

c. W

d. X

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47. Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

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

d. List of minimum equipment for efficient running of pharmacy

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48. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

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

d. Determine Possible therapeutic uses, Effective doses range

49 / 50

49. Patent Act is established in

a. 1940

b. 1948

c. 1919

d. 1970

50 / 50

50. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. Guidelines for clinical Trials

d. None of the above

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