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. Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Misbranded drugs

d. Ayurvedic drugs

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2. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Insecticide Act

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3. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

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

a. R1

b. R

c. O

d. S

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5. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. South Africa

d. Denmark

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6. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. India

d. Zimbabwe

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7. 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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8. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of incurable diseases

d. List of generic drugs

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

a. Every 6 year

b. Every 5 year

c. Every 3 year

d. Every 2 year

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10. 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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11. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Narcotic and psychotropic substance Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

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

a. Eight

b. Five

c. Six

d. Four

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

a. White

b. Yellow

c. Blue

d. Red

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

a. President of India

b. Government Analyst

c. The officer in charge of drugs control organization

d. Chief Administrator medical officer of state

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15. Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule P1

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16. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1954

d. 1948

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17. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

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

d. Determine Possible therapeutic uses, Effective doses range

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18. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

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

a. Q

b. FF

c. A

d. D

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

a. 3

b. 2

c. 1

d. 4

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

a. 250 square meters

b. 500 square meters

c. 150 square meters

d. 400 square meters

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22. 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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23. Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Barbital

d. Enalapril

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24. 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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25. Hatch Waxman Act is related to

a. Over the counter drugs

b. Banned drugs

c. Dangerous drugs Act

d. Spurious drugs Act

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

a. Six

b. Seven

c. Five

d. Nine

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

a. Ministry of Education

b. Central Government

c. Drug Controller

d. President, Pharmacy Council of India

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28. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule Y

d. Schedule G

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

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

b. Requirements of factory premises for the manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

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

a. 500 patients

b. 1-10 patients

c. 100 patients

d. 10-12 patients

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31. 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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32. 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 F

d. Schedule M

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

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

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34. Patent Act is established in

a. 1919

b. 1940

c. 1970

d. 1948

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

a. V

b. X

c. W

d. Y

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

a. 21B

b. 21

c. 20B

d. 20

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38. 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. True Drug

c. Misbranded Drug

d. Adulterated Drug

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39. Schedule N states

a. Standard for cosmetics

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

c. List of minimum equipment for efficient running of pharmacy

d. Requirement of factory premises and hygienic condition to complied

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40. 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. Chief pharmacist of government hospital

d. All

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Ophthalmic preparation

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42. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule P

d. Schedule A

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43. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule L

d. Schedule P

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

a. 1985

b. 1940

c. 1950

d. 1955

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45. 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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46. MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. UK

d. Brazil

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47. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase III

d. Phase V

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

a. In cold place

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

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

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49. 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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50. Dettol comes under

a. Schedule N

b. Schedule P

c. Schedule Q

d. Schedule O

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