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. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Requirement of factory premises and hygienic condition to complied

d. Standard for cosmetics

2 / 50

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

a. 150 square meters

b. 500 square meters

c. 400 square meters

d. 250 square meters

3 / 50

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

a. 10-12 patients

b. 500 patients

c. 1-10 patients

d. 100 patients

4 / 50

4. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

5 / 50

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

a. V

b. Y

c. W

d. X

6 / 50

6. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Spurious drugs Act

d. Banned drugs

7 / 50

7. 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

8 / 50

8. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

9 / 50

9. Coca, opium and hemp come under:

a. Poisons Act

b. Insecticide Act

c. Spurious Drug Act

d. Dangerous Drug Act

10 / 50

10. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 24

d. Form 27

11 / 50

11. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase V

d. Phase III

12 / 50

12. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule Q

d. Schedule P

13 / 50

13. Biological and Biotechnological products are included in schedule.

a. A

b. X

c. C and C1

d. B

14 / 50

14. List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule J

b. Schedule I

c. Schedule G

d. Schedule H

15 / 50

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

a. H

b. X

c. K

d. G

16 / 50

16. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

17 / 50

17. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

18 / 50

18. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

19 / 50

19. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Homeopathy product

d. List of Biological and Immunological product

20 / 50

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

a. Seven

b. Nine

c. Five

d. Six

21 / 50

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

a. 1950

b. 1955

c. 1940

d. 1985

22 / 50

22. MCC is regulatory agency of ……………

a. South Africa

b. Brazil

c. UK

d. Denmark

23 / 50

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

a. Red

b. Yellow

c. White

d. Blue

24 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Ophthalmic preparation

d. Skin cosmetic preparation

25 / 50

25. MHRA is regulatory agency of ……….....

a. Denmark

b. South Africa

c. Brazil

d. UK

26 / 50

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

a. Government Analyst

b. Chief Administrator medical officer of state

c. President of India

d. The officer in charge of drugs control organization

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. 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 H displayed on right top corner of the label.

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

d. Symbol X given in red

29 / 50

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

a. 4

b. 1

c. 3

d. 2

30 / 50

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

a. A cool place

b. A Cold place

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

d. Temperature not exceeding 5°C

31 / 50

31. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Enalapril

d. Metformin

32 / 50

32. 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

33 / 50

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

a. Six

b. Four

c. Five

d. Eight

34 / 50

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

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

b. At temperature which not exceed 20°C

c. At temperature which not exceed 5°C

d. In cold place

35 / 50

35. 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. Misbranded Drug

c. Adulterated Drug

d. Spurious Drug

36 / 50

36. TGA is regulatory agency of………….

a. Zimbabwe

b. Denmark

c. India

d. Australia

37 / 50

37. Schedule J is related to

a. GMP

b. Pack sizes of drugs.

c. Curable disease

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

38 / 50

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

a. Assistant drug controller

b. All

c. Chief pharmacist of government hospital

d. Chief administrative medical officer of the state

39 / 50

39. 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

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 required to open wholesale drug store

c. Area for opening retail pharmacy

d. List of maximum equipments for efficiently running pharmacy

41 / 50

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

a. A

b. D

c. Q

d. FF

42 / 50

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

a. R

b. R1

c. S

d. O

43 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 3 year

d. Every 2 year

44 / 50

44. 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 manufacture of Medical device

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

45 / 50

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

a. President, Pharmacy Council of India

b. Drug Controller

c. Ministry of Education

d. Central Government

46 / 50

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

a. Misbranded drugs

b. Toilet preparations

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

47 / 50

47. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule P

c. Schedule J

d. Schedule K

48 / 50

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

a. Requirements of factory premises

b. List of prescription drugs

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

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

49 / 50

49. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1985

d. 1954

50 / 50

50. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

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

d. Long time adverse effects aster marketing drug

Your score is

The average score is 37%