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. 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 Y

d. Schedule O

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2. 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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3. DTAB has ———————– ex officio members

a. Five

b. Six

c. Four

d. Eight

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

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5. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Insecticide Act

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. All

d. Chief administrative medical officer of the state

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7. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Dangerous drugs Act

d. Over the counter drugs

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8. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. C and C1

d. A

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9. 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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10. As per D and C act schedule T stated about

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

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

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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11. Patent Act is established in

a. 1919

b. 1948

c. 1970

d. 1940

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. President of India

d. Chief Administrator medical officer of state

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13. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

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

a. 2

b. 3

c. 4

d. 1

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15. 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. X

d. V

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16. 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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17. 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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18. 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 J

c. Schedule I

d. Schedule H

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19. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule B

d. Schedule A

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

a. Every 6 year

b. Every 3 year

c. Every 2 year

d. Every 5 year

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21. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule K

d. Schedule L

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22. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 24

c. Form 25

d. Form 26

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

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule Q

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

a. D

b. FF

c. A

d. Q

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25. MCC is regulatory agency of ……………

a. Brazil

b. Denmark

c. UK

d. South Africa

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26. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase III

d. Phase V

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

a. Central Government

b. President, Pharmacy Council of India

c. Drug Controller

d. Ministry of Education

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

a. Yellow

b. Blue

c. Red

d. White

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

a. Ayurvedic drugs

b. Toilet preparations

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

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30. Aspirin sodium comes under

a. Schedule H

b. Schedule G

c. Schedule Y

d. Schedule J

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

a. Brazil

b. UK

c. Denmark

d. South Africa

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

a. 250 square meters

b. 150 square meters

c. 500 square meters

d. 400 square meters

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33. 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. List of maximum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

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

a. A Cold place

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

c. Temperature not exceeding 5°C

d. A cool place

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35. 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. Adulterated Drug

c. True Drug

d. Misbranded Drug

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36. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Poisonous Act.

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37. 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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38. TGA is regulatory agency of………….

a. Australia

b. Zimbabwe

c. India

d. Denmark

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39. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1948

c. 1954

d. 1919

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

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

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

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

d. Symbol X given in red

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41. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule P

d. Schedule O

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

a. 1985

b. 1950

c. 1940

d. 1955

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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. 21

c. 20

d. 20B

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

a. S

b. O

c. R

d. R1

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46. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Ayurvedic product

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47. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Metformin

d. Enalapril

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48. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule O

d. Schedule R

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49. 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

50 / 50

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

a. Six

b. Nine

c. Five

d. Seven

Your score is

The average score is 37%