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

a. X

b. K

c. H

d. G

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2. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of generic drugs

c. Guidelines for clinical Trials

d. List of incurable diseases

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3. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule J

c. Schedule L

d. Schedule P

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

a. 21

b. 21B

c. 20B

d. 20

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5. 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 H displayed on right top corner of the label.

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

d. Symbol X given in red

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

a. X

b. Y

c. W

d. V

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7. Biological and Biotechnological products are included in schedule.

a. X

b. A

c. C and C1

d. B

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8. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

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

a. 150 square meters

b. 500 square meters

c. 250 square meters

d. 400 square meters

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10. 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. Government Analyst

d. Chief Administrator medical officer of state

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11. 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 Allopathy drugs

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

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

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12. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

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

a. Temperature not exceeding 5°C

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

c. A cool place

d. A Cold place

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

a. FF

b. Q

c. D

d. A

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15. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Brazil

d. Denmark

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16. Patent Act is established in

a. 1948

b. 1970

c. 1919

d. 1940

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

a. Yellow

b. Blue

c. Red

d. White

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18. 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 J

c. Schedule G

d. Schedule H

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

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule R

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

a. Six

b. Five

c. Four

d. Eight

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21. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase V

d. Phase III

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

a. 1940

b. 1955

c. 1950

d. 1985

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24. 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 F

c. Schedule O

d. Schedule Y

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25. Schedule J is related to

a. GMP

b. Pack sizes of drugs.

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

d. Curable disease

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

a. Every 2 year

b. Every 6 year

c. Every 3 year

d. Every 5 year

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27. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

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29. Dettol comes under

a. Schedule P

b. Schedule O

c. Schedule N

d. Schedule Q

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

a. 2

b. 4

c. 3

d. 1

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

a. Five

b. Seven

c. Six

d. Nine

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Ointment formulation

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

a. Chief administrative medical officer of the state

b. Chief pharmacist of government hospital

c. Assistant drug controller

d. All

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34. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule R

d. Schedule O

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35. 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 20°C

c. At temperature which not exceed 5°C

d. In cold place

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36. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 27

c. Form 26

d. Form 25

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

a. Denmark

b. Brazil

c. UK

d. South Africa

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39. In 1954 one of the following act is passed

a. Poisonous Act.

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

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

a. Area for opening retail pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

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

a. Schedule ‘C’ ‘G’ drugs

b. Ayurvedic drugs

c. Misbranded drugs

d. Toilet preparations

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42. Example of Schedule G drug is

a. Cefuroxime

b. Metformin

c. Enalapril

d. Barbital

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43. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1954

d. 1985

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44. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Dangerous drugs Act

d. Spurious drugs Act

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

a. O

b. R1

c. S

d. R

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46. Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule B

d. Schedule Q

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47. 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. Determine Possible therapeutic uses, Effective doses range

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

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48. TGA is regulatory agency of………….

a. India

b. Denmark

c. Australia

d. Zimbabwe

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

a. Central Government

b. Drug Controller

c. Ministry of Education

d. President, Pharmacy Council of India

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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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