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. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase V

c. Phase III

d. Phase I

2 / 50

2. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

3 / 50

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

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

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

c. Requirements of factory premises

d. List of prescription drugs

4 / 50

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

a. S

b. R

c. O

d. R1

5 / 50

5. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Metformin

d. Cefuroxime

6 / 50

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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ointment formulation

d. Ophthalmic preparation

7 / 50

7. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 24

d. Form 27

8 / 50

8. 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 J

c. Schedule H

d. Schedule I

9 / 50

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

a. 3

b. 4

c. 1

d. 2

10 / 50

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

a. White

b. Yellow

c. Red

d. Blue

11 / 50

11. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule P

d. Schedule O

12 / 50

12. Hatch Waxman Act is related to

a. Over the counter drugs

b. Banned drugs

c. Spurious drugs Act

d. Dangerous drugs Act

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 M

b. Schedule O

c. Schedule Y

d. Schedule F

14 / 50

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

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule Q

15 / 50

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

a. FF

b. D

c. A

d. Q

16 / 50

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

a. Every 2 year

b. Every 5 year

c. Every 6 year

d. Every 3 year

17 / 50

17. 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 Homeopathy drugs

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

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

18 / 50

18. Pack size of drug is covered under

a. Schedule P

b. Schedule R

c. Schedule P1

d. Schedule O

19 / 50

19. 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. Adulterated Drug

b. True Drug

c. Misbranded Drug

d. Spurious Drug

20 / 50

20. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

21 / 50

21. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1985

c. 1948

d. 1919

22 / 50

22. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule Q

d. Schedule P

23 / 50

23. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule L

d. Schedule K

24 / 50

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

a. V

b. X

c. Y

d. W

25 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Central Government

d. Drug Controller

26 / 50

26. In 1954 one of the following act is passed

a. Poisonous Act.

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Drug and magic Remedies Act

27 / 50

27. Schedule J is related to

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

b. Pack sizes of drugs.

c. GMP

d. Curable disease

28 / 50

28. 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

29 / 50

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

a. Nine

b. Seven

c. Six

d. Five

30 / 50

30. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule Y

d. Schedule H

31 / 50

31. 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

32 / 50

32. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Poisons Act

d. Spurious Drug Act

33 / 50

33. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of incurable diseases

c. None of the above

d. List of generic drugs

34 / 50

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

a. 1985

b. 1950

c. 1955

d. 1940

35 / 50

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

a. G

b. X

c. H

d. K

36 / 50

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

a. 500 patients

b. 10-12 patients

c. 1-10 patients

d. 100 patients

37 / 50

37. Patent Act is established in

a. 1948

b. 1970

c. 1919

d. 1940

38 / 50

38. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. C and C1

d. A

39 / 50

39. TGA is regulatory agency of………….

a. India

b. Australia

c. Denmark

d. Zimbabwe

40 / 50

40. 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. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

41 / 50

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

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

b. Symbol N 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

42 / 50

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

a. A Cold place

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

c. Temperature not exceeding 5°C

d. A cool place

43 / 50

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

a. Four

b. Eight

c. Six

d. Five

44 / 50

44. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

45 / 50

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

a. Ayurvedic drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Misbranded drugs

46 / 50

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

a. Chief pharmacist of government hospital

b. All

c. Assistant drug controller

d. Chief administrative medical officer of the state

47 / 50

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

a. At temperature which not exceed 20°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 5°C

48 / 50

48. Schedule C is related to

a. List of Homeopathy product

b. List of Allopathic product

c. List of Ayurvedic product

d. List of Biological and Immunological product

49 / 50

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

a. 20

b. 20B

c. 21

d. 21B

50 / 50

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

a. 500 square meters

b. 250 square meters

c. 150 square meters

d. 400 square meters

Your score is

The average score is 37%