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

359

1 / 50

1. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 25

c. Form 24

d. Form 26

2 / 50

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

a. R

b. S

c. O

d. R1

3 / 50

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

a. 1955

b. 1950

c. 1940

d. 1985

4 / 50

4. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

5 / 50

5. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase I

d. Phase II

6 / 50

6. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Dangerous Drug Act

c. Insecticide Act

d. Poisons Act

7 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Toilet preparations

d. Schedule ‘C’ ‘G’ drugs

8 / 50

8. 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 X given in red

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

9 / 50

9. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Brazil

d. Denmark

10 / 50

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

a. 250 square meters

b. 150 square meters

c. 500 square meters

d. 400 square meters

11 / 50

11. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1919

c. 1948

d. 1985

12 / 50

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

a. D

b. A

c. FF

d. Q

13 / 50

13. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

14 / 50

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

a. Five

b. Six

c. Nine

d. Seven

15 / 50

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

a. Schedule R

b. Schedule Q

c. Schedule O

d. Schedule P

16 / 50

16. 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. 20

d. 20B

17 / 50

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

a. Six

b. Five

c. Eight

d. Four

18 / 50

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

a. Area for opening retail pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. Area required to open wholesale drug store

d. List of minimum equipments for efficiently running pharmacy

19 / 50

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

a. Drug Controller

b. Central Government

c. President, Pharmacy Council of India

d. Ministry of Education

20 / 50

20. 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. W

d. Y

21 / 50

21. MHRA is regulatory agency of ……….....

a. Denmark

b. Brazil

c. South Africa

d. UK

22 / 50

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

a. Every 6 year

b. Every 3 year

c. Every 5 year

d. Every 2 year

23 / 50

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

a. Chief pharmacist of government hospital

b. All

c. Chief administrative medical officer of the state

d. Assistant drug controller

24 / 50

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

a. Requirements of factory premises

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

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

d. List of prescription drugs

25 / 50

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

a. In cold place

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

c. At temperature which not exceed 20°C

d. At temperature which not exceed 5°C

26 / 50

26. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

27 / 50

27. 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 Y

b. Schedule F

c. Schedule M

d. Schedule O

28 / 50

28. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of generic drugs

d. List of incurable diseases

29 / 50

29. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule P1

d. Schedule O

30 / 50

30. Schedule J is related to

a. Curable disease

b. GMP

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

d. Pack sizes of drugs.

31 / 50

31. Schedule C is related to

a. List of Ayurvedic product

b. List of Homeopathy product

c. List of Allopathic product

d. List of Biological and Immunological product

32 / 50

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

a. K

b. G

c. H

d. X

33 / 50

33. 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

34 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

35 / 50

35. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

36 / 50

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

a. A Cold place

b. Temperature not exceeding 5°C

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

d. A cool place

37 / 50

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

a. Yellow

b. Red

c. Blue

d. White

38 / 50

38. Schedule N states

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

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

39 / 50

39. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Enalapril

d. Metformin

40 / 50

40. Patent Act is established in

a. 1940

b. 1948

c. 1970

d. 1919

41 / 50

41. 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

42 / 50

42. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule B

d. Schedule A

43 / 50

43. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Drug and magic Remedies Act

d. Poisonous Act.

44 / 50

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

a. 4

b. 3

c. 2

d. 1

45 / 50

45. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule Q

d. Schedule P

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. True Drug

b. Spurious Drug

c. Misbranded Drug

d. Adulterated Drug

47 / 50

47. 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

48 / 50

48. Hatch Waxman Act is related to

a. Banned drugs

b. Dangerous drugs Act

c. Over the counter drugs

d. Spurious drugs Act

49 / 50

49. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule J

d. Schedule K

50 / 50

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

a. The officer in charge of drugs control organization

b. President of India

c. Government Analyst

d. Chief Administrator medical officer of state

Your score is

The average score is 37%