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

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

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

c. Symbol X given in red

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

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2. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Over the counter drugs

d. Spurious drugs Act

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3. MCC is regulatory agency of ……………

a. Denmark

b. UK

c. South Africa

d. Brazil

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

a. White

b. Red

c. Yellow

d. Blue

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5. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. Drug and magic Remedies Act

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

a. 20B

b. 21

c. 21B

d. 20

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

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

a. A cool place

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

c. A Cold place

d. Temperature not exceeding 5°C

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9. Biological and Biotechnological products are included in schedule.

a. B

b. C and C1

c. X

d. A

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

a. 1985

b. 1950

c. 1940

d. 1955

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

a. W

b. Y

c. V

d. X

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12. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule P1

d. Schedule O

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

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14. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 26

c. Form 25

d. Form 27

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

a. President, Pharmacy Council of India

b. Ministry of Education

c. Drug Controller

d. Central Government

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16. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. List of incurable diseases

d. None of the above

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17. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

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18. 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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19. 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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20. 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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21. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Barbital

d. Metformin

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22. 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. Chief Administrator medical officer of state

d. Government Analyst

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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. Spurious Drug

c. Misbranded Drug

d. Adulterated Drug

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24. 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 prescription drugs

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

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

a. 4

b. 3

c. 1

d. 2

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

a. In cold place

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

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

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27. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1985

d. 1919

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28. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. List of minimum equipment for efficient running of pharmacy

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

d. Standard for cosmetics

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29. As per D and C act schedule T stated about

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

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

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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30. 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 Y

c. Schedule F

d. Schedule M

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

a. R

b. S

c. O

d. R1

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

a. Every 2 year

b. Every 5 year

c. Every 3 year

d. Every 6 year

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. All

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34. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule K

c. Schedule L

d. Schedule P

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35. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule G

d. Schedule J

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

a. Nine

b. Six

c. Seven

d. Five

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37. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Poisons Act

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

a. Q

b. D

c. A

d. FF

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

a. X

b. H

c. G

d. K

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40. Schedule C is related to

a. List of Homeopathy product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Allopathic product

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41. 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 I

c. Schedule G

d. Schedule J

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42. Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule B

d. Schedule P

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

a. 500 square meters

b. 250 square meters

c. 150 square meters

d. 400 square meters

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44. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

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45. 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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46. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. South Africa

d. UK

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

a. Schedule R

b. Schedule Q

c. Schedule P

d. Schedule O

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48. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule N

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49. Patent Act is established in

a. 1948

b. 1919

c. 1970

d. 1940

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

a. Eight

b. Four

c. Five

d. Six

Your score is

The average score is 38%