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. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

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

a. 1

b. 2

c. 3

d. 4

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3. Injection syringe and needles are covered under

a. Schedule B

b. Schedule Q

c. Schedule P

d. Schedule A

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4. 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. W

d. X

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

a. 1940

b. 1985

c. 1950

d. 1955

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

a. 500 patients

b. 10-12 patients

c. 1-10 patients

d. 100 patients

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

a. 400 square meters

b. 500 square meters

c. 250 square meters

d. 150 square meters

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8. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule P1

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

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10. Biological and Biotechnological products are included in schedule.

a. C and C1

b. B

c. X

d. A

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11. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule K

c. Schedule P

d. Schedule J

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

a. 21

b. 20

c. 21B

d. 20B

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13. 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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14. Schedule D as per D & C Act is concerned with

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

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

c. List of prescription drugs

d. Requirements of factory premises

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15. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

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

a. Five

b. Nine

c. Six

d. Seven

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17. Schedule C is related to

a. List of Biological and Immunological product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Allopathic product

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18. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. South Africa

d. UK

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

a. Five

b. Four

c. Six

d. Eight

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20. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 24

c. Form 25

d. Form 26

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. President of India

d. Government Analyst

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

a. Schedule R

b. Schedule Q

c. Schedule O

d. Schedule P

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

a. S

b. R

c. O

d. R1

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24. 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. True Drug

b. Misbranded Drug

c. Spurious Drug

d. Adulterated Drug

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25. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of incurable diseases

c. None of the above

d. List of generic drugs

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26. Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule Y

d. Schedule H

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27. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

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28. Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

c. GMP

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

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29. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Poisons Act

c. Spurious Drug Act

d. Insecticide Act

30 / 50

30. TGA is regulatory agency of………….

a. Zimbabwe

b. Denmark

c. Australia

d. India

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

a. Toilet preparations

b. Misbranded drugs

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

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32. 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 manufacturer of Homeopathy drugs

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

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

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33. 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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34. In 1954 one of the following act is passed

a. Poisonous Act.

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Drug and magic Remedies Act

35 / 50

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

36 / 50

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

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

b. A Cold place

c. A cool place

d. Temperature not exceeding 5°C

37 / 50

37. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Banned drugs

d. Spurious drugs Act

38 / 50

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

a. A

b. D

c. FF

d. Q

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

a. White

b. Red

c. Yellow

d. Blue

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

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

b. Symbol X given in red

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

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

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

a. All

b. Chief administrative medical officer of the state

c. Chief pharmacist of government hospital

d. Assistant drug controller

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42. 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 I

c. Schedule H

d. Schedule J

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Central Government

d. Ministry of Education

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45. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

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

a. X

b. G

c. K

d. H

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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 F

c. Schedule M

d. Schedule O

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48. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

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49. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

50 / 50

50. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase I

d. Phase II

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The average score is 38%

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