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

a. Assistant drug controller

b. Chief administrative medical officer of the state

c. All

d. Chief pharmacist of government hospital

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2. 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. Adulterated Drug

d. True Drug

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

a. The officer in charge of drugs control organization

b. President of India

c. Chief Administrator medical officer of state

d. Government Analyst

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4. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

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5. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

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6. Pack size of drug is covered under

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule P1

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

a. Toilet preparations

b. Misbranded drugs

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

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8. 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 5°C

c. At temperature which not exceed 20°C

d. In cold place

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

a. 1985

b. 1955

c. 1940

d. 1950

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10. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. Guidelines for clinical Trials

d. None of the above

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11. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule P

c. Schedule L

d. Schedule J

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

a. H

b. G

c. X

d. K

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13. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

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

a. A

b. D

c. Q

d. FF

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

a. Red

b. White

c. Blue

d. Yellow

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

a. 250 square meters

b. 400 square meters

c. 500 square meters

d. 150 square meters

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17. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

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18. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule P

d. Schedule O

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19. Schedule J is related to

a. Pack sizes of drugs.

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

c. Curable disease

d. GMP

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20. 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. W

d. X

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

a. A cool place

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

c. A Cold place

d. Temperature not exceeding 5°C

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22. As per D and C act schedule T stated about

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

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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

a. 2

b. 1

c. 4

d. 3

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

a. List of maximum equipments for efficiently running pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. Area for opening retail pharmacy

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25. 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 I

c. Schedule H

d. Schedule G

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

a. Seven

b. Five

c. Nine

d. Six

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27. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

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

a. 20

b. 20B

c. 21

d. 21B

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

a. Five

b. Eight

c. Four

d. Six

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30. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 27

d. Form 25

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31. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Barbital

d. Metformin

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

a. Schedule R

b. Schedule Q

c. Schedule P

d. Schedule O

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33. 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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34. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

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

a. 500 patients

b. 10-12 patients

c. 100 patients

d. 1-10 patients

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36. 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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37. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule Y

d. Schedule H

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38. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. South Africa

d. Denmark

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39. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

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40. 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 O

d. Schedule Y

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41. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Biological and Immunological product

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

a. O

b. R1

c. S

d. R

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43. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

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44. 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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45. Pharmacy Council of India (PCI) is reconstituted:

a. Every 5 year

b. Every 3 year

c. Every 6 year

d. Every 2 year

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46. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

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

a. Australia

b. India

c. Denmark

d. Zimbabwe

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49. 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 X given in red

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

50 / 50

50. Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule B

d. Schedule P

Your score is

The average score is 38%