Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law And Ethics DPEE Noteskarts

Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law and Ethics DPEE

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

Top 50 Question for Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law and Ethics DPEE

358

1 / 50

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

a. W

b. X

c. V

d. Y

2 / 50

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. List of maximum equipments for efficiently running pharmacy

3 / 50

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

a. Drug Controller

b. Ministry of Education

c. President, Pharmacy Council of India

d. Central Government

4 / 50

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

a. Schedule O

b. Schedule Q

c. Schedule R

d. Schedule P

5 / 50

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

a. 3

b. 2

c. 1

d. 4

6 / 50

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

a. White

b. Yellow

c. Blue

d. Red

7 / 50

7. MHRA is regulatory agency of ……….....

a. South Africa

b. Brazil

c. UK

d. Denmark

8 / 50

8. 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

9 / 50

9. 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 G

c. Schedule I

d. Schedule J

10 / 50

10. 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 H displayed on right top corner of the label.

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

d. Symbol X given in red

11 / 50

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

a. 400 square meters

b. 250 square meters

c. 500 square meters

d. 150 square meters

12 / 50

12. 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

13 / 50

13. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

14 / 50

14. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. Denmark

d. UK

15 / 50

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

a. Misbranded drugs

b. Schedule ‘C’ ‘G’ drugs

c. Ayurvedic drugs

d. Toilet preparations

16 / 50

16. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Insecticide Act

17 / 50

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

a. 100 patients

b. 1-10 patients

c. 10-12 patients

d. 500 patients

18 / 50

18. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Cefuroxime

d. Barbital

19 / 50

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

a. D

b. FF

c. Q

d. A

20 / 50

20. 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

21 / 50

21. TGA is regulatory agency of………….

a. Denmark

b. India

c. Australia

d. Zimbabwe

22 / 50

22. 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

23 / 50

23. Schedule J is related to

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

b. Curable disease

c. GMP

d. Pack sizes of drugs.

24 / 50

24. Pack size of drug is covered under

a. Schedule O

b. Schedule R

c. Schedule P

d. Schedule P1

25 / 50

25. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule P

c. Schedule J

d. Schedule L

26 / 50

26. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Homeopathy product

d. List of Ayurvedic product

27 / 50

27. 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. 21

d. 21B

28 / 50

28. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

29 / 50

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

a. R1

b. O

c. S

d. R

30 / 50

30. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. X

d. C and C1

31 / 50

31. Patent Act is established in

a. 1919

b. 1970

c. 1940

d. 1948

32 / 50

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

a. Nine

b. Six

c. Five

d. Seven

33 / 50

33. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule N

d. Schedule Q

34 / 50

34. In 1954 one of the following act is passed

a. Poisonous Act.

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

35 / 50

35. 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

36 / 50

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

a. President of India

b. Chief Administrator medical officer of state

c. Government Analyst

d. The officer in charge of drugs control organization

37 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 5 year

d. Every 3 year

38 / 50

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

a. G

b. K

c. X

d. H

39 / 50

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

a. 1985

b. 1950

c. 1955

d. 1940

40 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

41 / 50

41. 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

42 / 50

42. Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule Q

d. Schedule A

43 / 50

43. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Spurious drugs Act

c. Banned drugs

d. Over the counter drugs

44 / 50

44. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

45 / 50

45. 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

46 / 50

46. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule J

d. Schedule G

47 / 50

47. 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

48 / 50

48. 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. Spurious Drug

c. True Drug

d. Adulterated Drug

49 / 50

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

a. Four

b. Six

c. Eight

d. Five

50 / 50

50. Schedule N states

a. Standard for cosmetics

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

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

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