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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ointment formulation

d. Ophthalmic preparation

2 / 50

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

d. Symbol X given in red

3 / 50

3. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

4 / 50

4. 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

5 / 50

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

a. Schedule P

b. Schedule Q

c. Schedule R

d. Schedule O

6 / 50

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

a. All

b. Chief pharmacist of government hospital

c. Chief administrative medical officer of the state

d. Assistant drug controller

7 / 50

7. In 1954 one of the following act is passed

a. Poisonous Act.

b. Narcotic and psychotropic substance Act

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

8 / 50

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

a. Red

b. Blue

c. Yellow

d. White

9 / 50

9. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

10 / 50

10. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Barbital

d. Metformin

11 / 50

11. 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

12 / 50

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

a. At temperature which not exceed 5°C

b. At temperature which not exceed 20°C

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

d. In cold place

13 / 50

13. 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 O

d. Schedule Y

14 / 50

14. Coca, opium and hemp come under:

a. Poisons Act

b. Dangerous Drug Act

c. Insecticide Act

d. Spurious Drug Act

15 / 50

15. 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

16 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

17 / 50

17. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. Brazil

d. UK

18 / 50

18. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1954

d. 1948

19 / 50

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

a. O

b. S

c. R1

d. R

20 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 6 year

d. Every 2 year

21 / 50

21. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

22 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

c. A cool place

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

23 / 50

23. Schedule J is related to

a. Pack sizes of drugs.

b. Curable disease

c. GMP

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

24 / 50

24. Schedule C is related to

a. List of Homeopathy product

b. List of Biological and Immunological product

c. List of Allopathic product

d. List of Ayurvedic product

25 / 50

25. 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. Long time adverse effects aster marketing drug

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

26 / 50

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

a. 4

b. 1

c. 2

d. 3

27 / 50

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

a. Seven

b. Nine

c. Six

d. Five

28 / 50

28. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

29 / 50

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

a. X

b. K

c. G

d. H

30 / 50

30. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 26

d. Form 27

31 / 50

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

a. 1985

b. 1940

c. 1950

d. 1955

32 / 50

32. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule P1

33 / 50

33. Biological and Biotechnological products are included in schedule.

a. B

b. X

c. A

d. C and C1

34 / 50

34. 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. Spurious Drug

c. Misbranded Drug

d. Adulterated Drug

35 / 50

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

a. 21B

b. 20

c. 20B

d. 21

36 / 50

36. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule K

d. Schedule J

37 / 50

37. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule Q

d. Schedule P

38 / 50

38. TGA is regulatory agency of………….

a. India

b. Australia

c. Zimbabwe

d. Denmark

39 / 50

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

a. W

b. Y

c. X

d. V

40 / 50

40. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Standard for cosmetics

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

d. Requirement of factory premises and hygienic condition to complied

41 / 50

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

a. Five

b. Eight

c. Four

d. Six

42 / 50

42. 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

43 / 50

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

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

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

c. Requirements of factory premises for the manufacturer of Allopathy drugs

d. Requirements of factory premises for the manufacturer of Homeopathy drugs

44 / 50

44. Patent Act is established in

a. 1948

b. 1940

c. 1970

d. 1919

45 / 50

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

a. D

b. Q

c. FF

d. A

46 / 50

46. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. List of generic drugs

c. None of the above

d. Guidelines for clinical Trials

47 / 50

47. 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

48 / 50

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

a. President of India

b. Chief Administrator medical officer of state

c. The officer in charge of drugs control organization

d. Government Analyst

49 / 50

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

a. 500 square meters

b. 400 square meters

c. 250 square meters

d. 150 square meters

50 / 50

50. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Over the counter drugs

c. Banned drugs

d. Dangerous drugs Act

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The average score is 37%