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 / 50

1. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

2 / 50

2. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

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3. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. None of the above

d. Guidelines for clinical Trials

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

a. Six

b. Four

c. Eight

d. Five

5 / 50

5. Patent Act is established in

a. 1940

b. 1970

c. 1919

d. 1948

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6. Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

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

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7. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

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8. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Denmark

d. Brazil

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9. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

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10. 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 is red displayed on left top corner of the label

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

d. Symbol X given in red

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11. 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 M

b. Schedule F

c. Schedule Y

d. Schedule O

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12. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule P

d. Schedule K

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13. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Banned drugs

d. Dangerous drugs Act

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

a. S

b. R

c. R1

d. O

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

a. President, Pharmacy Council of India

b. Central Government

c. Drug Controller

d. Ministry of Education

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

a. Ophthalmic preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Parenteral preparation

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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 I

b. Schedule J

c. Schedule G

d. Schedule H

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19. Coca, opium and hemp come under:

a. Insecticide Act

b. Spurious Drug Act

c. Poisons Act

d. Dangerous Drug Act

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

a. 1950

b. 1985

c. 1940

d. 1955

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21. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

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

a. Red

b. Yellow

c. Blue

d. White

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23. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1919

d. 1954

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

a. Schedule O

b. Schedule P

c. Schedule R

d. Schedule Q

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26. 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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27. 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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28. Schedule D as per D & C Act is concerned with

a. List of prescription drugs

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

c. Requirements of factory premises

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

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

a. Seven

b. Nine

c. Six

d. Five

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

a. List of maximum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

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31. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Cefuroxime

d. Barbital

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32. 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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33. 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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34. Pharmacy Council of India contain comprises…….. Members (s) from AICTE and UGC.

a. 4

b. 1

c. 2

d. 3

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35. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule N

d. Schedule Q

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

a. Q

b. A

c. D

d. FF

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

a. W

b. X

c. V

d. Y

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

a. All

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. Assistant drug controller

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40. TGA is regulatory agency of………….

a. Australia

b. Zimbabwe

c. India

d. Denmark

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41. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Homeopathy product

d. List of Ayurvedic product

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42. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule P1

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43. Schedule J is related to

a. Pack sizes of drugs.

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

c. GMP

d. Curable disease

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Misbranded drugs

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45. 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. Spurious Drug

c. Misbranded Drug

d. True Drug

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46. 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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47. Insulin injection according to schedule P is should be stored

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

b. At temperature which not exceed 20°C

c. In cold place

d. At temperature which not exceed 5°C

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48. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. X

d. A

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

a. 10-12 patients

b. 1-10 patients

c. 100 patients

d. 500 patients

50 / 50

50. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule J

d. Schedule G

Your score is

The average score is 38%