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. 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. In cold place

c. At temperature which not exceed 5°C

d. At temperature which not exceed 20°C

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2. 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 X given in red

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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3. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

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4. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Banned drugs

d. Spurious drugs Act

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

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

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6. 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 F

b. Schedule Y

c. Schedule M

d. Schedule O

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7. Schedule C is related to

a. List of Ayurvedic product

b. List of Biological and Immunological product

c. List of Allopathic product

d. List of Homeopathy product

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8. MCC is regulatory agency of ……………

a. Denmark

b. South Africa

c. UK

d. Brazil

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9. 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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10. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule J

d. Schedule P

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11. Schedule J is related to

a. Pack sizes of drugs.

b. GMP

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

d. Curable disease

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

a. S

b. O

c. R

d. R1

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13. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule P

d. Schedule O

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

a. 1985

b. 1940

c. 1950

d. 1955

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

a. 1-10 patients

b. 10-12 patients

c. 100 patients

d. 500 patients

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

a. Five

b. Six

c. Seven

d. Nine

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

a. Requirements of factory premises

b. List of prescription drugs

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

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

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

a. White

b. Red

c. Blue

d. Yellow

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19. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Poisons Act

d. Spurious Drug Act

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20. In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. The Medical Termination of pregnancy Act

d. Drug and magic Remedies Act

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21. 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. 20B

d. 21B

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22. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase III

d. Phase I

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

a. Four

b. Five

c. Six

d. Eight

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24. TGA is regulatory agency of………….

a. Zimbabwe

b. India

c. Australia

d. Denmark

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

a. Ayurvedic drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

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26. 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. Misbranded Drug

b. Adulterated Drug

c. Spurious Drug

d. True Drug

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27. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

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

a. 250 square meters

b. 400 square meters

c. 150 square meters

d. 500 square meters

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29. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule H

d. Schedule J

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30. 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 J

c. Schedule I

d. Schedule H

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31. 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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32. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule A

d. Schedule P

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33. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Metformin

d. Enalapril

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34. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule N

d. Schedule O

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

a. FF

b. A

c. Q

d. D

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36. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

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

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37. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

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38. 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

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Ophthalmic preparation

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40. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. X

d. B

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

a. Chief administrative medical officer of the state

b. Assistant drug controller

c. All

d. Chief pharmacist of government hospital

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

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule R

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

a. Government Analyst

b. President of India

c. The officer in charge of drugs control organization

d. Chief Administrator medical officer of state

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44. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

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45. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1985

c. 1948

d. 1919

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

a. 4

b. 2

c. 1

d. 3

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47. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of incurable diseases

c. List of generic drugs

d. None of the above

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

a. G

b. K

c. X

d. H

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Ministry of Education

d. Central Government

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50. 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 Allopathy drugs

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

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

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