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

350

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1. 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 G

d. Schedule H

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

a. O

b. S

c. R1

d. R

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3. 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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4. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. Narcotic and psychotropic substance Act

d. The Medical Termination of pregnancy Act

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5. Schedule N states

a. Standard for cosmetics

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

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

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6. 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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7. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

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8. 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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9. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. X

d. B

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10. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule K

d. Schedule J

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

a. Every 5 year

b. Every 6 year

c. Every 2 year

d. Every 3 year

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

a. 100 patients

b. 1-10 patients

c. 500 patients

d. 10-12 patients

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13. 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. W

d. V

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14. 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. 20

d. 20B

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

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

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

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

d. Symbol X given in red

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16. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1954

c. 1948

d. 1985

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17. 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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18. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. Denmark

d. UK

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

a. Schedule Q

b. Schedule R

c. Schedule O

d. Schedule P

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

a. 2

b. 1

c. 4

d. 3

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22. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 24

c. Form 26

d. Form 25

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23. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Dangerous Drug Act

d. Insecticide Act

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

a. Red

b. White

c. Yellow

d. Blue

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

a. K

b. H

c. G

d. X

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

a. 500 square meters

b. 250 square meters

c. 400 square meters

d. 150 square meters

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28. 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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29. MHRA is regulatory agency of ……….....

a. UK

b. Denmark

c. Brazil

d. South Africa

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. President of India

d. Chief Administrator medical officer of state

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

a. 1950

b. 1985

c. 1955

d. 1940

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32. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. Guidelines for clinical Trials

c. List of generic drugs

d. None of the above

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Ministry of Education

d. Central Government

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34. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

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

a. Five

b. Four

c. Eight

d. Six

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36. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

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37. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase V

d. Phase I

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38. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule P

d. Schedule O

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

a. Ayurvedic drugs

b. Toilet preparations

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

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40. 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 Allopathy drugs

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

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

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41. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule P

d. Schedule O

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42. 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. Misbranded Drug

b. Adulterated Drug

c. Spurious Drug

d. True Drug

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

a. FF

b. D

c. Q

d. A

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44. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Metformin

d. Enalapril

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

a. Six

b. Five

c. Nine

d. Seven

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46. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. Zimbabwe

d. India

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. All

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

a. Requirements of factory premises

b. List of prescription drugs

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

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

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