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

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

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

c. List of prescription drugs

d. Requirements of factory premises

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2. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule P

c. Schedule J

d. Schedule L

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3. MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. Brazil

d. UK

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4. 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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5. 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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6. 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 5°C

d. At temperature which not exceed 20°C

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

a. Q

b. A

c. D

d. FF

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8. Patent Act is established in

a. 1919

b. 1948

c. 1940

d. 1970

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9. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Banned drugs

c. Over the counter drugs

d. Dangerous drugs Act

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

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

a. Central Government

b. Ministry of Education

c. President, Pharmacy Council of India

d. Drug Controller

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

a. O

b. R1

c. R

d. S

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14. 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. Misbranded Drug

c. Adulterated Drug

d. Spurious Drug

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

a. Schedule R

b. Schedule Q

c. Schedule O

d. Schedule P

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16. 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 M

c. Schedule Y

d. Schedule O

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17. 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 H

c. Schedule G

d. Schedule J

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18. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

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

a. 400 square meters

b. 150 square meters

c. 500 square meters

d. 250 square meters

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20. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. Australia

d. India

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

a. Eight

b. Four

c. Six

d. Five

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

a. Every 5 year

b. Every 3 year

c. Every 2 year

d. Every 6 year

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23. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase I

c. Phase II

d. Phase V

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

a. 1

b. 4

c. 3

d. 2

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

a. White

b. Red

c. Yellow

d. Blue

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26. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. List of incurable diseases

d. Guidelines for clinical Trials

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27. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

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28. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

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

d. Long time adverse effects aster marketing drug

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

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

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30. 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. Area required to open wholesale drug store

d. List of minimum equipments for efficiently running pharmacy

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31. Schedule J is related to

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

b. Pack sizes of drugs.

c. Curable disease

d. GMP

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32. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1985

d. 1919

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

a. 10-12 patients

b. 1-10 patients

c. 100 patients

d. 500 patients

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. President of India

d. The officer in charge of drugs control organization

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35. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Metformin

d. Cefuroxime

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36. Schedule C is related to

a. List of Biological and Immunological product

b. List of Allopathic product

c. List of Ayurvedic product

d. List of Homeopathy product

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37. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Poisons Act

d. Spurious Drug Act

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

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

a. Temperature not exceeding 5°C

b. A cool place

c. A Cold place

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

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41. Schedule N states

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

b. Standard for cosmetics

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

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42. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule Y

d. Schedule H

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43. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

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

a. Five

b. Seven

c. Six

d. Nine

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

a. Chief pharmacist of government hospital

b. All

c. Assistant drug controller

d. Chief administrative medical officer of the state

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46. Injection syringe and needles are covered under

a. Schedule A

b. Schedule Q

c. Schedule B

d. Schedule P

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47. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

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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. K

b. X

c. H

d. G

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

a. 1940

b. 1955

c. 1950

d. 1985

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50. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 27

d. Form 25

Your score is

The average score is 37%