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. 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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2. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. List of incurable diseases

d. Guidelines for clinical Trials

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3. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Banned drugs

d. Dangerous drugs Act

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4. 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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5. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule J

c. Schedule P

d. Schedule L

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

a. Six

b. Eight

c. Five

d. Four

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7. 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

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8. 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 Y

b. Schedule M

c. Schedule O

d. Schedule F

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

a. Q

b. FF

c. D

d. A

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10. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

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11. 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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12. 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. A Cold place

c. A cool place

d. Temperature not exceeding 5°C

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13. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Poisons Act

d. Spurious Drug Act

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

a. Every 2 year

b. Every 6 year

c. Every 3 year

d. Every 5 year

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15. 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 X given in red

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

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

a. Seven

b. Six

c. Nine

d. Five

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17. TGA is regulatory agency of………….

a. India

b. Denmark

c. Australia

d. Zimbabwe

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18. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

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19. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1985

c. 1948

d. 1919

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20. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

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

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21. 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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22. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

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23. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

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24. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Denmark

d. Brazil

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

a. S

b. O

c. R1

d. R

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

a. 1985

b. 1955

c. 1940

d. 1950

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27. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 26

d. Form 24

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

a. Requirements of factory premises

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

c. List of prescription drugs

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

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29. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

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

a. 150 square meters

b. 500 square meters

c. 250 square meters

d. 400 square meters

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31. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule Q

d. Schedule P

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

a. 1-10 patients

b. 10-12 patients

c. 500 patients

d. 100 patients

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

a. Y

b. W

c. V

d. X

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. President of India

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36. 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. True Drug

b. Spurious Drug

c. Adulterated Drug

d. Misbranded Drug

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

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38. 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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39. 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 Allopathy drugs

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

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

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

a. 1

b. 2

c. 4

d. 3

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41. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

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42. 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 G

c. Schedule J

d. Schedule H

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

a. 21B

b. 20B

c. 20

d. 21

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44. 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. H

d. X

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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ointment formulation

d. Ophthalmic preparation

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46. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule P

d. Schedule O

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47. Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Metformin

d. Barbital

48 / 50

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

a. Red

b. Yellow

c. White

d. Blue

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49. Schedule J is related to

a. Curable disease

b. GMP

c. Pack sizes of drugs.

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

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50. 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)

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