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

a. 400 square meters

b. 150 square meters

c. 250 square meters

d. 500 square meters

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

a. In cold place

b. At temperature which not exceed 5°C

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

d. At temperature which not exceed 20°C

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

a. R1

b. R

c. S

d. O

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5. Schedule C is related to

a. List of Ayurvedic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Allopathic product

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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. W

b. X

c. Y

d. V

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

a. Five

b. Nine

c. Six

d. Seven

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8. Patent Act is established in

a. 1940

b. 1919

c. 1970

d. 1948

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9. TGA is regulatory agency of………….

a. India

b. Denmark

c. Australia

d. Zimbabwe

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

a. Q

b. A

c. D

d. FF

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

a. Ointment formulation

b. Parenteral preparation

c. Ophthalmic preparation

d. Skin cosmetic preparation

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12. Injection syringe and needles are covered under

a. Schedule P

b. Schedule A

c. Schedule Q

d. Schedule B

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13. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

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

a. Schedule Q

b. Schedule O

c. Schedule R

d. Schedule P

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15. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 24

d. Form 25

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16. 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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17. 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 Ayurveda, Sidhha and Unani drugs

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

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

a. All

b. Chief pharmacist of government hospital

c. Assistant drug controller

d. Chief administrative medical officer of the state

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

a. List of minimum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

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20. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

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21. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

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22. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Dangerous Drug Act

d. Poisons Act

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23. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. C and C1

d. A

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24. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Spurious drugs Act

d. Banned drugs

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25. MCC is regulatory agency of ……………

a. Brazil

b. Denmark

c. South Africa

d. UK

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

a. Every 3 year

b. Every 5 year

c. Every 2 year

d. Every 6 year

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27. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of incurable diseases

d. List of generic drugs

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

a. Toilet preparations

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Ayurvedic drugs

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29. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

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30. Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

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

d. GMP

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

a. Symbol X given in red

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 H displayed on right top corner of the label.

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32. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Barbital

d. Cefuroxime

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33. 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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34. 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 M

c. Schedule F

d. Schedule O

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

a. 1-10 patients

b. 10-12 patients

c. 500 patients

d. 100 patients

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

a. Four

b. Six

c. Eight

d. Five

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37. 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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38. In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

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39. MHRA is regulatory agency of ……….....

a. Brazil

b. UK

c. South Africa

d. Denmark

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40. 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. 20

d. 20B

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

a. Yellow

b. White

c. Blue

d. Red

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

a. 4

b. 3

c. 1

d. 2

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

a. 1985

b. 1950

c. 1940

d. 1955

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

a. Chief Administrator medical officer of state

b. The officer in charge of drugs control organization

c. Government Analyst

d. President of India

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46. 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 G

c. Schedule H

d. Schedule J

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47. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase III

d. Phase V

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48. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule R

d. Schedule O

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

a. G

b. H

c. K

d. X

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50. 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. True Drug

d. Adulterated Drug

Your score is

The average score is 37%