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 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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2. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule O

d. Schedule P

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

a. Symbol X given in red

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

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

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

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

a. Chief pharmacist of government hospital

b. Assistant drug controller

c. Chief administrative medical officer of the state

d. All

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

d. Determine Possible therapeutic uses, Effective doses range

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

a. 1940

b. 1985

c. 1950

d. 1955

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7. Patent Act is established in

a. 1948

b. 1970

c. 1919

d. 1940

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8. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule K

d. Schedule J

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. The officer in charge of drugs control organization

d. President of India

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10. Schedule J is related to

a. GMP

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

c. Pack sizes of drugs.

d. Curable disease

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

a. Eight

b. Five

c. Four

d. Six

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12. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. C and C1

d. A

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

a. S

b. R1

c. O

d. R

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14. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule A

c. Schedule B

d. Schedule P

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15. 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 F

c. Schedule Y

d. Schedule M

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16. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of incurable diseases

c. Guidelines for clinical Trials

d. List of generic drugs

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17. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 24

d. Form 25

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18. 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 manufacturer of Ayurveda, Sidhha and Unani 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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19. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

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

a. Parenteral preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Skin cosmetic preparation

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21. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Metformin

d. Enalapril

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

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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. Misbranded Drug

b. Spurious Drug

c. True Drug

d. Adulterated Drug

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

d. List of prescription drugs

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26. Hatch Waxman Act is related to

a. Banned drugs

b. Dangerous drugs Act

c. Over the counter drugs

d. Spurious drugs Act

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27. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1919

d. 1948

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

a. Y

b. W

c. X

d. V

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29. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

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

a. Every 6 year

b. Every 2 year

c. Every 3 year

d. Every 5 year

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

a. 250 square meters

b. 150 square meters

c. 400 square meters

d. 500 square meters

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32. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

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33. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Poisons Act

d. Spurious Drug Act

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

a. Blue

b. Red

c. White

d. Yellow

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35. Pack size of drug is covered under

a. Schedule R

b. Schedule P1

c. Schedule O

d. Schedule P

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36. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase I

d. Phase V

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37. 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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38. 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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39. Pharmacy Council of India contain comprises…….. Members (s) from AICTE and UGC.

a. 3

b. 4

c. 1

d. 2

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40. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. South Africa

d. UK

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Central Government

d. Drug Controller

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

a. Schedule P

b. Schedule R

c. Schedule Q

d. Schedule O

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43. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Homeopathy product

d. List of Biological and Immunological product

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

a. D

b. Q

c. A

d. FF

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45. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

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

a. Temperature not exceeding 5°C

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

c. A cool place

d. A Cold place

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

a. Six

b. Five

c. Seven

d. Nine

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48. 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. 21B

d. 20B

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49. Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule H

d. Schedule G

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50. 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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