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. 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 X given in red

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

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

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

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

b. Requirements of factory premises

c. List of prescription drugs

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

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

a. Every 3 year

b. Every 2 year

c. Every 6 year

d. Every 5 year

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4. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Poisons Act

d. Spurious Drug Act

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5. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. List of incurable diseases

d. Guidelines for clinical Trials

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

a. Temperature not exceeding 5°C

b. A Cold place

c. A cool place

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

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

a. Chief administrative medical officer of the state

b. Assistant drug controller

c. All

d. Chief pharmacist of government hospital

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9. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

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10. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule K

c. Schedule J

d. Schedule P

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

a. 4

b. 2

c. 1

d. 3

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12. 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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13. For parenteral preparation in glass containers minimum area required is

a. 150 square meters

b. 250 square meters

c. 500 square meters

d. 400 square meters

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14. 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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15. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 26

d. Form 24

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16. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

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17. Purpose of Phase-3 trial is

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

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

c. Determine Possible therapeutic uses, Effective doses range

d. Long time adverse effects aster marketing drug

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

a. R

b. S

c. O

d. R1

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19. 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. X

d. W

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20. 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. In cold place

d. At temperature which not exceed 20°C

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21. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Banned drugs

c. Dangerous drugs Act

d. Over the counter drugs

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22. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

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

a. Q

b. FF

c. A

d. D

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

a. Seven

b. Five

c. Six

d. Nine

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25. Schedule J is related to

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

b. GMP

c. Pack sizes of drugs.

d. Curable disease

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

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

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

a. 21B

b. 20B

c. 21

d. 20

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28. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

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

a. Six

b. Eight

c. Five

d. Four

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30. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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31. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule J

d. Schedule G

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

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33. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule Q

d. Schedule O

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34. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule P

d. Schedule O

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35. 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. Misbranded Drug

c. True Drug

d. Spurious Drug

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36. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

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37. 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 manufacture of Medical device

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

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

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

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39. Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule A

d. Schedule Q

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40. 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 H

c. Schedule J

d. Schedule I

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

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule R

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

a. H

b. K

c. X

d. G

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43. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. X

d. C and C1

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. The officer in charge of drugs control organization

d. President of India

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

a. Red

b. Yellow

c. Blue

d. White

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

a. 10-12 patients

b. 1-10 patients

c. 500 patients

d. 100 patients

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47. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Drug and magic Remedies Act

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

a. 1940

b. 1985

c. 1950

d. 1955

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49. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1954

d. 1919

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50. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

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