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 first edition of India Pharmacopoeia was published in the year :

a. 1955

b. 1985

c. 1950

d. 1940

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

a. Nine

b. Five

c. Six

d. Seven

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

a. Every 3 year

b. Every 6 year

c. Every 5 year

d. Every 2 year

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4. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1948

c. 1954

d. 1919

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

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6. Dettol comes under

a. Schedule P

b. Schedule Q

c. Schedule N

d. Schedule O

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7. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Metformin

d. Cefuroxime

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

a. Symbol X given in red

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

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

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

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9. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. B

d. C and C1

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

a. 4

b. 1

c. 3

d. 2

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

a. A cool place

b. A Cold place

c. Temperature not exceeding 5°C

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

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12. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

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13. 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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14. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase I

d. Phase III

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

a. A

b. FF

c. Q

d. D

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16. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 24

c. Form 26

d. Form 25

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

a. Toilet preparations

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

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18. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of incurable diseases

c. Guidelines for clinical Trials

d. List of generic drugs

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19. Hatch Waxman Act is related to

a. Banned drugs

b. Dangerous drugs Act

c. Spurious drugs Act

d. Over the counter drugs

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20. Schedule J is related to

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

b. Pack sizes of drugs.

c. GMP

d. Curable disease

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

a. W

b. Y

c. X

d. V

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

a. Drug Controller

b. Central Government

c. President, Pharmacy Council of India

d. Ministry of Education

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23. Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule Y

d. Schedule H

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24. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Spurious Drug Act

d. Dangerous Drug Act

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25. 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 Y

c. Schedule O

d. Schedule F

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26. 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 manufacture of Medical device

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

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

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27. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. UK

d. Denmark

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

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29. 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. True Drug

d. Misbranded Drug

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

a. X

b. H

c. K

d. G

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

a. In cold place

b. At temperature which not exceed 5°C

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

d. At temperature which not exceed 20°C

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

a. R1

b. O

c. S

d. R

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

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34. Schedule C is related to

a. List of Ayurvedic product

b. List of Biological and Immunological product

c. List of Homeopathy product

d. List of Allopathic product

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35. 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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36. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule P

d. Schedule O

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

a. Red

b. Yellow

c. White

d. Blue

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38. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

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

a. President of India

b. Chief Administrator medical officer of state

c. The officer in charge of drugs control organization

d. Government Analyst

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40. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

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41. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

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42. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

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

a. 100 patients

b. 10-12 patients

c. 500 patients

d. 1-10 patients

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

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45. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

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46. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule P

d. Schedule L

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47. 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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48. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. South Africa

d. Denmark

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

a. Five

b. Six

c. Four

d. Eight

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

a. Chief pharmacist of government hospital

b. All

c. Chief administrative medical officer of the state

d. Assistant drug controller

Your score is

The average score is 38%