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

356

1 / 50

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

a. Seven

b. Five

c. Six

d. Nine

2 / 50

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

a. White

b. Red

c. Yellow

d. Blue

3 / 50

3. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1954

c. 1948

d. 1985

4 / 50

4. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

5 / 50

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

a. 500 patients

b. 1-10 patients

c. 100 patients

d. 10-12 patients

6 / 50

6. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule N

d. Schedule P

7 / 50

7. 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

8 / 50

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

a. A

b. FF

c. Q

d. D

9 / 50

9. Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

10 / 50

10. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. None of the above

d. List of incurable diseases

11 / 50

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

12 / 50

12. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Poisons Act

d. Spurious Drug Act

13 / 50

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

a. 20B

b. 21B

c. 21

d. 20

14 / 50

14. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

15 / 50

15. 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

16 / 50

16. 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.

17 / 50

17. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

18 / 50

18. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

19 / 50

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

a. Drug Controller

b. Ministry of Education

c. Central Government

d. President, Pharmacy Council of India

20 / 50

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. The officer in charge of drugs control organization

d. President of India

21 / 50

21. 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 F

c. Schedule M

d. Schedule Y

22 / 50

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

a. 2

b. 3

c. 1

d. 4

23 / 50

23. Schedule J is related to

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

b. Curable disease

c. Pack sizes of drugs.

d. GMP

24 / 50

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

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

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 manufacture of Medical device

25 / 50

25. 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

26 / 50

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

a. Eight

b. Four

c. Six

d. Five

27 / 50

27. TGA is regulatory agency of………….

a. India

b. Australia

c. Denmark

d. Zimbabwe

28 / 50

28. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule P

d. Schedule R

29 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 5 year

d. Every 3 year

30 / 50

30. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

31 / 50

31. Hatch Waxman Act is related to

a. Banned drugs

b. Dangerous drugs Act

c. Over the counter drugs

d. Spurious drugs Act

32 / 50

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

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

33 / 50

33. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Metformin

d. Cefuroxime

34 / 50

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

a. Temperature not exceeding 5°C

b. A cool place

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

d. A Cold place

35 / 50

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

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule Q

36 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

37 / 50

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

a. 250 square meters

b. 150 square meters

c. 400 square meters

d. 500 square meters

38 / 50

38. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

39 / 50

39. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

40 / 50

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

a. X

b. W

c. V

d. Y

41 / 50

41. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule J

c. Schedule P

d. Schedule K

42 / 50

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

a. S

b. O

c. R1

d. R

43 / 50

43. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

44 / 50

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ointment formulation

d. Ophthalmic preparation

45 / 50

45. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

46 / 50

46. 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. Misbranded Drug

c. True Drug

d. Spurious Drug

47 / 50

47. Schedule C is related to

a. List of Homeopathy product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Allopathic product

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 I

b. Schedule G

c. Schedule H

d. Schedule J

49 / 50

49. Injection syringe and needles are covered under

a. Schedule B

b. Schedule P

c. Schedule A

d. Schedule Q

50 / 50

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

a. Toilet preparations

b. Misbranded drugs

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

Your score is

The average score is 38%