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. K

b. H

c. G

d. X

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2. Insulin injection according to schedule P is should be stored

a. In cold place

b. At temperature which not exceed 20°C

c. At temperature which not exceed 5°C

d. At the Temperature 2°C to 8°C and it must not allow to freeze

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

a. Requirements of factory premises

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

c. List of prescription drugs

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

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4. 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 O

c. Schedule F

d. Schedule Y

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

a. R1

b. R

c. S

d. O

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6. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule K

d. Schedule L

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7. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1919

d. 1954

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

a. President of India

b. The officer in charge of drugs control organization

c. Government Analyst

d. Chief Administrator medical officer of state

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

a. 1-10 patients

b. 500 patients

c. 100 patients

d. 10-12 patients

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10. MHRA is regulatory agency of ……….....

a. Brazil

b. UK

c. South Africa

d. Denmark

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11. 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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12. 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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13. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

c. Determine Possible therapeutic uses, Effective doses range

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

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

a. Four

b. Six

c. Five

d. Eight

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Misbranded drugs

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

a. Skin cosmetic preparation

b. Ophthalmic preparation

c. Ointment formulation

d. Parenteral preparation

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

a. A

b. FF

c. D

d. Q

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18. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

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19. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule G

d. Schedule J

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20. Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Barbital

d. Metformin

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21. 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 N is red displayed on left 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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22. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

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24. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule O

d. Schedule Q

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

a. List of maximum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. Area required to open wholesale drug store

d. List of minimum equipments for efficiently running pharmacy

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26. 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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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. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase I

d. Phase V

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

a. V

b. W

c. Y

d. X

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

a. 1950

b. 1940

c. 1985

d. 1955

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32. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule R

d. Schedule O

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33. 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 Homeopathy drugs

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

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

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34. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Poisonous Act.

c. Narcotic and psychotropic substance Act

d. Drug and magic Remedies Act

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35. 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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36. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule Q

d. Schedule P

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

a. 500 square meters

b. 400 square meters

c. 250 square meters

d. 150 square meters

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38. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. Guidelines for clinical Trials

d. List of generic drugs

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

a. Blue

b. White

c. Red

d. Yellow

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40. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 24

d. Form 25

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41. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

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42. 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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43. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Denmark

d. Brazil

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

a. Drug Controller

b. Ministry of Education

c. President, Pharmacy Council of India

d. Central Government

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

a. 4

b. 2

c. 3

d. 1

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46. Patent Act is established in

a. 1948

b. 1919

c. 1940

d. 1970

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

a. A Cold place

b. A cool place

c. Temperature not exceeding 5°C

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

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

a. Seven

b. Nine

c. Six

d. Five

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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. Spurious Drug

d. Misbranded Drug

50 / 50

50. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Poisons Act

c. Spurious Drug Act

d. Insecticide Act

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The average score is 38%