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. Hatch Waxman Act is related to

a. Over the counter drugs

b. Banned drugs

c. Dangerous drugs Act

d. Spurious drugs Act

2 / 50

2. 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 H

c. Schedule I

d. Schedule J

3 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Skin cosmetic preparation

d. Ointment formulation

4 / 50

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

a. Ayurvedic drugs

b. Toilet preparations

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

5 / 50

5. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule K

c. Schedule P

d. Schedule J

6 / 50

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

a. 20B

b. 20

c. 21B

d. 21

7 / 50

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

8 / 50

8. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. C and C1

d. A

9 / 50

9. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

10 / 50

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

a. Yellow

b. Red

c. White

d. Blue

11 / 50

11. 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

12 / 50

12. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase II

d. Phase I

13 / 50

13. 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

14 / 50

14. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 27

c. Form 25

d. Form 24

15 / 50

15. Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

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

d. Requirement of factory premises and hygienic condition to complied

16 / 50

16. Aspirin sodium comes under

a. Schedule G

b. Schedule J

c. Schedule H

d. Schedule Y

17 / 50

17. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

18 / 50

18. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. None of the above

d. List of incurable diseases

19 / 50

19. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

20 / 50

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

a. Every 3 year

b. Every 2 year

c. Every 6 year

d. Every 5 year

21 / 50

21. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. Drug and magic Remedies Act

22 / 50

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

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

23 / 50

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. All

24 / 50

24. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

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

d. Long time adverse effects aster marketing drug

25 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

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

d. A cool place

26 / 50

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

a. Six

b. Five

c. Nine

d. Seven

27 / 50

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

a. 4

b. 2

c. 3

d. 1

28 / 50

28. MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. UK

d. Brazil

29 / 50

29. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1954

c. 1948

d. 1919

30 / 50

30. Patent Act is established in

a. 1970

b. 1948

c. 1919

d. 1940

31 / 50

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

a. S

b. R

c. O

d. R1

32 / 50

32. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule Q

d. Schedule P

33 / 50

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

c. Symbol X given in red

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

34 / 50

34. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Biological and Immunological product

35 / 50

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Central Government

d. Ministry of Education

36 / 50

36. 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 M

b. Schedule Y

c. Schedule F

d. Schedule O

37 / 50

37. 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

38 / 50

38. MCC is regulatory agency of ……………

a. Denmark

b. UK

c. South Africa

d. Brazil

39 / 50

39. 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. True Drug

c. Adulterated Drug

d. Spurious Drug

40 / 50

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

a. D

b. A

c. FF

d. Q

41 / 50

41. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

42 / 50

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

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule Q

43 / 50

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

a. 1940

b. 1955

c. 1950

d. 1985

44 / 50

44. Insulin injection according to schedule P is should be stored

a. At temperature which not exceed 5°C

b. In cold place

c. At the Temperature 2°C to 8°C and it must not allow to freeze

d. At temperature which not exceed 20°C

45 / 50

45. Schedule J is related to

a. Pack sizes of drugs.

b. GMP

c. Curable disease

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

46 / 50

46. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

47 / 50

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

a. K

b. G

c. X

d. H

48 / 50

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

a. Eight

b. Six

c. Five

d. Four

49 / 50

49. 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

50 / 50

50. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Denmark

d. Australia

Your score is

The average score is 38%