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

345

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1. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule P

d. Schedule O

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2. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

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3. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1948

c. 1954

d. 1919

4 / 50

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

a. 20B

b. 20

c. 21

d. 21B

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

a. Every 6 year

b. Every 2 year

c. Every 5 year

d. Every 3 year

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6. 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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7. 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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8. Schedule…………… of Drugs and Cosmetics Act in Cludes requirements and guidelines on clinical trials for import and manufacturing of new drugs.

a. Y

b. X

c. V

d. W

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

a. Nine

b. Seven

c. Six

d. Five

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10. Patent Act is established in

a. 1948

b. 1940

c. 1919

d. 1970

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11. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Spurious Drug Act

d. Poisons Act

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12. Aspirin sodium comes under

a. Schedule H

b. Schedule G

c. Schedule Y

d. Schedule J

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

a. S

b. R

c. R1

d. O

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14. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule K

d. Schedule L

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

a. A

b. Q

c. D

d. FF

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17. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Allopathic product

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18. 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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19. For parenteral preparation in glass containers minimum area required is

a. 400 square meters

b. 150 square meters

c. 500 square meters

d. 250 square meters

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20. 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 O

b. Schedule Y

c. Schedule F

d. Schedule M

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21. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Australia

d. Denmark

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

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

a. 1950

b. 1940

c. 1955

d. 1985

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24. Injection syringe and needles are covered under

a. Schedule B

b. Schedule Q

c. Schedule P

d. Schedule A

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25. 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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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 Allopathy drugs

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

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27. 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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28. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Standard for cosmetics

c. Requirement of factory premises and hygienic condition to complied

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

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

a. Symbol X given in red

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

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

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

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31. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

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

a. Yellow

b. Red

c. Blue

d. White

33 / 50

33. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of incurable diseases

d. List of generic drugs

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

a. Schedule ‘C’ ‘G’ drugs

b. Ayurvedic drugs

c. Toilet preparations

d. Misbranded drugs

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35. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule O

d. Schedule Q

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

a. Schedule G

b. Schedule J

c. Schedule I

d. Schedule H

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37. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Metformin

d. Enalapril

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

a. Temperature not exceeding 5°C

b. A cool place

c. A Cold place

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

39 / 50

39. Schedule J is related to

a. Pack sizes of drugs.

b. Curable disease

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

d. GMP

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

a. G

b. X

c. H

d. K

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

a. Government Analyst

b. Chief Administrator medical officer of state

c. President of India

d. The officer in charge of drugs control organization

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

a. 100 patients

b. 500 patients

c. 10-12 patients

d. 1-10 patients

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43. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 24

c. Form 25

d. Form 26

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

a. 4

b. 3

c. 2

d. 1

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

a. Eight

b. Six

c. Five

d. Four

46 / 50

46. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

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

a. Denmark

b. Brazil

c. South Africa

d. UK

48 / 50

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

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule R

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49. 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. True Drug

c. Misbranded Drug

d. Spurious Drug

50 / 50

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

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

b. List of prescription drugs

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

d. Requirements of factory premises

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