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

364

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

a. List of prescription drugs

b. Requirements of factory premises

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

a. Eight

b. Five

c. Four

d. Six

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

a. 1950

b. 1955

c. 1985

d. 1940

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4. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule P

d. Schedule Q

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5. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1985

d. 1919

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6. 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 Homeopathy drugs

c. Requirements of factory premises for the manufacturer of Ayurveda, Sidhha and Unani drugs

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

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

a. O

b. R1

c. R

d. S

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

a. 500 patients

b. 100 patients

c. 1-10 patients

d. 10-12 patients

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9. 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. True Drug

c. Adulterated Drug

d. Misbranded Drug

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10. 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. At temperature which not exceed 5°C

c. At temperature which not exceed 20°C

d. In cold place

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

a. Six

b. Nine

c. Five

d. Seven

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12. TGA is regulatory agency of………….

a. Zimbabwe

b. India

c. Australia

d. Denmark

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13. 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. 21

d. 21B

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14. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

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15. 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. Chief pharmacist of government hospital

d. All

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16. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Over the counter drugs

d. Banned drugs

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

a. List of minimum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

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

a. Schedule J

b. Schedule I

c. Schedule G

d. Schedule H

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

a. A cool place

b. Temperature not exceeding 5°C

c. A Cold place

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

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21. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule R

d. Schedule P

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22. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase V

d. Phase I

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23. 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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24. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Allopathic product

d. List of Biological and Immunological product

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

a. Toilet preparations

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

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26. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. UK

d. Brazil

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27. 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 M

d. Schedule F

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28. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Poisonous Act.

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

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

a. Schedule P

b. Schedule R

c. Schedule O

d. Schedule Q

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30. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. List of incurable diseases

c. List of generic drugs

d. Guidelines for clinical Trials

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31. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

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

a. A

b. D

c. FF

d. Q

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33. Injection syringe and needles are covered under

a. Schedule B

b. Schedule Q

c. Schedule P

d. Schedule A

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34. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 24

d. Form 26

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35. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Denmark

d. Brazil

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36. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Metformin

d. Enalapril

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

a. Skin cosmetic preparation

b. Ophthalmic preparation

c. Ointment formulation

d. Parenteral preparation

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

a. Blue

b. Yellow

c. Red

d. White

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39. Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

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

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

a. Every 2 year

b. Every 6 year

c. Every 3 year

d. Every 5 year

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41. Patent Act is established in

a. 1948

b. 1970

c. 1919

d. 1940

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42. 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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43. 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. W

d. V

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

a. 3

b. 4

c. 1

d. 2

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

a. Central Government

b. President, Pharmacy Council of India

c. Drug Controller

d. Ministry of Education

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46. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Insecticide Act

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

a. 250 square meters

b. 500 square meters

c. 400 square meters

d. 150 square meters

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48. 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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49. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule K

d. Schedule J

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

a. X

b. K

c. G

d. H

Your score is

The average score is 38%