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. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

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

a. Schedule R

b. Schedule P

c. Schedule Q

d. Schedule O

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

a. Chief Administrator medical officer of state

b. President of India

c. Government Analyst

d. The officer in charge of drugs control organization

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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. Drug and magic Remedies Act

d. Narcotic and psychotropic substance Act

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

a. 4

b. 3

c. 2

d. 1

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

a. Drug Controller

b. President, Pharmacy Council of India

c. Central Government

d. Ministry of Education

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

a. 1985

b. 1950

c. 1955

d. 1940

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

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

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10. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 26

c. Form 27

d. Form 25

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11. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule N

d. Schedule P

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

a. At temperature which not exceed 20°C

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

c. At temperature which not exceed 5°C

d. In cold place

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13. List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule J

b. Schedule G

c. Schedule H

d. Schedule I

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

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15. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Poisons Act

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16. MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. UK

d. Brazil

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17. 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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18. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. A

d. C and C1

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19. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

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21. 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 Homeopathy drugs

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

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

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22. 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 O

c. Schedule M

d. Schedule F

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23. 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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24. Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule P1

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

a. Six

b. Seven

c. Nine

d. Five

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

a. Eight

b. Four

c. Six

d. Five

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27. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Cefuroxime

d. Barbital

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28. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

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29. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Homeopathy product

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

a. 400 square meters

b. 500 square meters

c. 250 square meters

d. 150 square meters

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31. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

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

a. 20B

b. 21

c. 21B

d. 20

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

a. Toilet preparations

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Ayurvedic drugs

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34. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1948

d. 1985

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

a. G

b. H

c. K

d. X

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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. Misbranded Drug

b. Spurious Drug

c. True Drug

d. Adulterated Drug

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37. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

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38. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Brazil

d. Denmark

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39. Schedule J is related to

a. GMP

b. Curable disease

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

d. Pack sizes of drugs.

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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. V

b. Y

c. X

d. W

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41. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule J

d. Schedule K

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

a. Red

b. White

c. Yellow

d. Blue

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43. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

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44. 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 N displayed on left top corner of the label.

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

d. Symbol X given in red

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45. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. Guidelines for clinical Trials

c. List of generic drugs

d. None of the above

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

a. Q

b. A

c. FF

d. D

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

a. 1-10 patients

b. 500 patients

c. 10-12 patients

d. 100 patients

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

a. O

b. R1

c. R

d. S

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

a. Temperature not exceeding 5°C

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

c. A cool place

d. A Cold place

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50. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

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

d. List of minimum equipment for efficient running of pharmacy

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The average score is 38%