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. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Spurious Drug Act

d. Poisons Act

2 / 50

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

a. President, Pharmacy Council of India

b. Central Government

c. Ministry of Education

d. Drug Controller

3 / 50

3. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. The Medical Termination of pregnancy Act

d. Narcotic and psychotropic substance Act

4 / 50

4. 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

5 / 50

5. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

6 / 50

6. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase I

d. Phase V

7 / 50

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

a. Five

b. Nine

c. Six

d. Seven

8 / 50

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. All

9 / 50

9. 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. Spurious Drug

b. True Drug

c. Misbranded Drug

d. Adulterated Drug

10 / 50

10. 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.

11 / 50

11. 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 F

c. Schedule Y

d. Schedule O

12 / 50

12. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule Y

d. Schedule H

13 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

14 / 50

14. Dettol comes under

a. Schedule Q

b. Schedule O

c. Schedule N

d. Schedule P

15 / 50

15. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

16 / 50

16. Patent Act is established in

a. 1948

b. 1919

c. 1970

d. 1940

17 / 50

17. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule B

d. Schedule A

18 / 50

18. MCC is regulatory agency of ……………

a. Denmark

b. South Africa

c. Brazil

d. UK

19 / 50

19. MHRA is regulatory agency of ……….....

a. South Africa

b. Denmark

c. UK

d. Brazil

20 / 50

20. 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

21 / 50

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

a. D

b. FF

c. Q

d. A

22 / 50

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

a. Ointment formulation

b. Parenteral preparation

c. Ophthalmic preparation

d. Skin cosmetic preparation

23 / 50

23. Schedule N states

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

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

d. Standard for cosmetics

24 / 50

24. TGA is regulatory agency of………….

a. Australia

b. India

c. Zimbabwe

d. Denmark

25 / 50

25. 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

26 / 50

26. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1948

d. 1954

27 / 50

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

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

28 / 50

28. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule L

d. Schedule K

29 / 50

29. 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

30 / 50

30. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Banned drugs

c. Dangerous drugs Act

d. Over the counter drugs

31 / 50

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

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule R

32 / 50

32. 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 X given in red

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

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

33 / 50

33. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. B

d. A

34 / 50

34. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Ayurvedic product

35 / 50

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

a. Blue

b. White

c. Yellow

d. Red

36 / 50

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

a. Misbranded drugs

b. Ayurvedic drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

37 / 50

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

a. 3

b. 2

c. 4

d. 1

38 / 50

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

a. 21B

b. 21

c. 20B

d. 20

39 / 50

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

a. 100 patients

b. 500 patients

c. 10-12 patients

d. 1-10 patients

40 / 50

40. 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

41 / 50

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

a. 1950

b. 1955

c. 1985

d. 1940

42 / 50

42. 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

43 / 50

43. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Metformin

d. Enalapril

44 / 50

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

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

b. Temperature not exceeding 5°C

c. A cool place

d. A Cold place

45 / 50

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

a. R1

b. O

c. R

d. S

46 / 50

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

a. 500 square meters

b. 250 square meters

c. 400 square meters

d. 150 square meters

47 / 50

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

a. Y

b. W

c. V

d. X

48 / 50

48. 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 I

c. Schedule J

d. Schedule G

49 / 50

49. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

50 / 50

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

a. Four

b. Six

c. Eight

d. Five

Your score is

The average score is 37%