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. 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. 20

d. 21B

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2. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

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

a. Seven

b. Six

c. Five

d. Nine

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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ophthalmic preparation

d. Ointment formulation

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5. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Poisonous Act.

c. Narcotic and psychotropic substance Act

d. Drug and magic Remedies Act

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6. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

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

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Toilet preparations

d. Ayurvedic drugs

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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 O

b. Schedule M

c. Schedule F

d. Schedule Y

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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. K

b. H

c. G

d. X

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

a. Chief administrative medical officer of the state

b. All

c. Assistant drug controller

d. Chief pharmacist of government hospital

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11. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

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12. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

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13. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. Guidelines for clinical Trials

d. List of generic drugs

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

a. 4

b. 1

c. 2

d. 3

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15. 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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16. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

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17. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule R

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

a. In cold place

b. At temperature which not exceed 20°C

c. At temperature which not exceed 5°C

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

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

a. Yellow

b. Blue

c. Red

d. White

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22. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule B

d. Schedule A

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23. 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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24. TGA is regulatory agency of………….

a. Zimbabwe

b. India

c. Denmark

d. Australia

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25. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. B

d. A

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26. Patent Act is established in

a. 1948

b. 1919

c. 1970

d. 1940

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27. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Barbital

d. Cefuroxime

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28. Schedule J is related to

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

b. GMP

c. Pack sizes of drugs.

d. Curable disease

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

a. Symbol X given in red

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

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

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

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31. 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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32. 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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33. 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. True Drug

d. Adulterated Drug

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34. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Banned drugs

c. Dangerous drugs Act

d. Over the counter drugs

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35. MHRA is regulatory agency of ……….....

a. Denmark

b. UK

c. Brazil

d. South Africa

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36. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase III

d. Phase I

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37. 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 H

c. Schedule J

d. Schedule G

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

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39. 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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40. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1948

c. 1985

d. 1919

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41. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule O

d. Schedule N

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

a. R1

b. O

c. R

d. S

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43. Pack size of drug is covered under

a. Schedule O

b. Schedule P1

c. Schedule P

d. Schedule R

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44. 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. Requirements of factory premises

c. List of prescription drugs

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

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

a. Four

b. Five

c. Eight

d. Six

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

a. D

b. A

c. FF

d. Q

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

a. 1950

b. 1985

c. 1940

d. 1955

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

a. 100 patients

b. 500 patients

c. 1-10 patients

d. 10-12 patients

50 / 50

50. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Poisons Act

d. Spurious Drug Act

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The average score is 38%