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 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Skin cosmetic preparation

2 / 50

2. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

3 / 50

3. 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

4 / 50

4. 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 cool place

c. Temperature not exceeding 5°C

d. A Cold place

5 / 50

5. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. Zimbabwe

d. India

6 / 50

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

a. A

b. D

c. Q

d. FF

7 / 50

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

a. 10-12 patients

b. 1-10 patients

c. 500 patients

d. 100 patients

8 / 50

8. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

9 / 50

9. 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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10. 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 manufacturer of Homeopathy drugs

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

11 / 50

11. 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 20°C

d. At temperature which not exceed 5°C

12 / 50

12. 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

13 / 50

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

a. 1

b. 3

c. 4

d. 2

14 / 50

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

a. 21

b. 21B

c. 20

d. 20B

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15. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

16 / 50

16. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

17 / 50

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

a. 1955

b. 1940

c. 1985

d. 1950

18 / 50

18. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

19 / 50

19. MHRA is regulatory agency of ……….....

a. South Africa

b. Denmark

c. UK

d. Brazil

20 / 50

20. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

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21. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule O

d. Schedule P

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22. Biological and Biotechnological products are included in schedule.

a. B

b. C and C1

c. X

d. A

23 / 50

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

a. Red

b. White

c. Blue

d. Yellow

24 / 50

24. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. UK

d. South Africa

25 / 50

25. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase II

c. Phase I

d. Phase III

26 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

27 / 50

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

a. Drug Controller

b. Ministry of Education

c. Central Government

d. President, Pharmacy Council of India

28 / 50

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

a. Every 5 year

b. Every 2 year

c. Every 6 year

d. Every 3 year

29 / 50

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

a. Five

b. Six

c. Four

d. Eight

30 / 50

30. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 24

d. Form 26

31 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Misbranded drugs

d. Ayurvedic drugs

32 / 50

32. Patent Act is established in

a. 1970

b. 1940

c. 1948

d. 1919

33 / 50

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. President of India

d. Government Analyst

34 / 50

34. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

35 / 50

35. 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 Y

b. Schedule F

c. Schedule M

d. Schedule O

36 / 50

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

a. R

b. R1

c. O

d. S

37 / 50

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

a. H

b. X

c. K

d. G

38 / 50

38. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Enalapril

d. Metformin

39 / 50

39. Coca, opium and hemp come under:

a. Poisons Act

b. Insecticide Act

c. Spurious Drug Act

d. Dangerous Drug Act

40 / 50

40. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

41 / 50

41. 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. Adulterated Drug

c. True Drug

d. Misbranded Drug

42 / 50

42. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of incurable diseases

d. List of generic drugs

43 / 50

43. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1954

d. 1948

44 / 50

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

a. Nine

b. Seven

c. Five

d. Six

45 / 50

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

a. W

b. V

c. X

d. Y

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

47 / 50

47. 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

48 / 50

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

a. 150 square meters

b. 500 square meters

c. 400 square meters

d. 250 square meters

49 / 50

49. 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 X given in red

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

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

50 / 50

50. 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 J

c. Schedule I

d. Schedule G

Your score is

The average score is 37%