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. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

2 / 50

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

a. Ophthalmic preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Parenteral preparation

3 / 50

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

a. Every 6 year

b. Every 5 year

c. Every 3 year

d. Every 2 year

4 / 50

4. Patent Act is established in

a. 1970

b. 1919

c. 1948

d. 1940

5 / 50

5. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

6 / 50

6. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. UK

d. South Africa

7 / 50

7. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Dangerous drugs Act

d. Spurious drugs Act

8 / 50

8. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

9 / 50

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

a. At temperature which not exceed 20°C

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

c. In cold place

d. At temperature which not exceed 5°C

10 / 50

10. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

11 / 50

11. 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

12 / 50

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

a. 20

b. 21

c. 20B

d. 21B

13 / 50

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

a. 500 square meters

b. 150 square meters

c. 250 square meters

d. 400 square meters

14 / 50

14. TGA is regulatory agency of………….

a. Australia

b. India

c. Zimbabwe

d. Denmark

15 / 50

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

a. Seven

b. Five

c. Six

d. Nine

16 / 50

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

a. Drug Controller

b. President, Pharmacy Council of India

c. Ministry of Education

d. Central Government

17 / 50

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

a. Misbranded drugs

b. Toilet preparations

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

18 / 50

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

a. 1-10 patients

b. 500 patients

c. 100 patients

d. 10-12 patients

19 / 50

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

20 / 50

20. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. Guidelines for clinical Trials

d. List of generic drugs

21 / 50

21. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule Q

d. Schedule P

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22. 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. Adulterated Drug

c. Spurious Drug

d. Misbranded Drug

23 / 50

23. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1985

c. 1919

d. 1948

24 / 50

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

a. Six

b. Eight

c. Five

d. Four

25 / 50

25. 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

26 / 50

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

a. Red

b. Blue

c. Yellow

d. White

27 / 50

27. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Biological and Immunological product

28 / 50

28. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Poisons Act

29 / 50

29. 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 F

d. Schedule M

30 / 50

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

a. Symbol X given in red

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

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

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

31 / 50

31. Aspirin sodium comes under

a. Schedule H

b. Schedule G

c. Schedule J

d. Schedule Y

32 / 50

32. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. Poisonous Act.

33 / 50

33. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule P1

34 / 50

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

a. The officer in charge of drugs control organization

b. President of India

c. Chief Administrator medical officer of state

d. Government Analyst

35 / 50

35. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Cefuroxime

d. Metformin

36 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

37 / 50

37. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule Q

d. Schedule P

38 / 50

38. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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. Determine Possible therapeutic uses, Effective doses range

39 / 50

39. 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

40 / 50

40. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase I

d. Phase V

41 / 50

41. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

42 / 50

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

a. 2

b. 4

c. 3

d. 1

43 / 50

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

a. Y

b. V

c. W

d. X

44 / 50

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

a. Schedule R

b. Schedule O

c. Schedule Q

d. Schedule P

45 / 50

45. 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 J

d. Schedule H

46 / 50

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

a. 1950

b. 1985

c. 1955

d. 1940

47 / 50

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

a. D

b. FF

c. Q

d. A

48 / 50

48. Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

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

d. GMP

49 / 50

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

a. S

b. R

c. O

d. R1

50 / 50

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

a. All

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. Chief pharmacist of government hospital

Your score is

The average score is 38%