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

a. A Cold place

b. Temperature not exceeding 5°C

c. A cool place

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

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2. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

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

a. A

b. D

c. Q

d. FF

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4. 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. List of minimum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

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

a. Government Analyst

b. President of India

c. Chief Administrator medical officer of state

d. The officer in charge of drugs control organization

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6. Injection syringe and needles are covered under

a. Schedule P

b. Schedule A

c. Schedule Q

d. Schedule B

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

a. Skin cosmetic preparation

b. Ophthalmic preparation

c. Parenteral preparation

d. Ointment formulation

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

a. White

b. Blue

c. Yellow

d. Red

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9. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule R

d. Schedule P

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10. 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. V

d. W

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

a. 10-12 patients

b. 500 patients

c. 100 patients

d. 1-10 patients

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

a. Requirements of factory premises

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

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

d. List of prescription drugs

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13. 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 manufacture of Medical device

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

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

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14. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

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15. Schedule C is related to

a. List of Biological and Immunological product

b. List of Allopathic product

c. List of Ayurvedic product

d. List of Homeopathy product

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

a. 150 square meters

b. 400 square meters

c. 500 square meters

d. 250 square meters

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17. 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 O

b. Schedule M

c. Schedule Y

d. Schedule F

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18. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

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

a. President, Pharmacy Council of India

b. Ministry of Education

c. Central Government

d. Drug Controller

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

a. Five

b. Six

c. Eight

d. Four

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

a. Every 2 year

b. Every 3 year

c. Every 5 year

d. Every 6 year

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22. List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule H

b. Schedule J

c. Schedule I

d. Schedule G

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23. 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. Adulterated Drug

c. Misbranded Drug

d. Spurious Drug

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

d. Determine Possible therapeutic uses, Effective doses range

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25. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1948

d. 1954

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

a. R1

b. S

c. O

d. R

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27. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase III

d. Phase II

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

a. 20

b. 20B

c. 21B

d. 21

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

a. K

b. G

c. X

d. H

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

a. Seven

b. Five

c. Six

d. Nine

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

a. 2

b. 3

c. 4

d. 1

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32. MHRA is regulatory agency of ……….....

a. South Africa

b. Brazil

c. Denmark

d. UK

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33. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

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34. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule G

d. Schedule J

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35. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Spurious drugs Act

d. Dangerous drugs Act

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36. Schedule J is related to

a. Pack sizes of drugs.

b. Curable disease

c. GMP

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

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37. Patent Act is established in

a. 1940

b. 1948

c. 1919

d. 1970

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38. Coca, opium and hemp come under:

a. Insecticide Act

b. Spurious Drug Act

c. Poisons Act

d. Dangerous Drug Act

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39. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. List of generic drugs

c. None of the above

d. Guidelines for clinical Trials

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40. 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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41. MCC is regulatory agency of ……………

a. Denmark

b. South Africa

c. Brazil

d. UK

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42. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. B

d. X

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

a. At temperature which not exceed 5°C

b. At temperature which not exceed 20°C

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

d. In cold place

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44. Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Metformin

d. Barbital

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45. 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 N displayed on left top corner of the label.

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

d. Symbol X given in red

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

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47. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

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48. 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. Assistant drug controller

d. Chief pharmacist of government hospital

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

a. 1955

b. 1985

c. 1940

d. 1950

50 / 50

50. Dettol comes under

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule N

Your score is

The average score is 38%