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

a. R

b. S

c. O

d. R1

2 / 50

2. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of incurable diseases

d. List of generic drugs

3 / 50

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

a. 2

b. 1

c. 4

d. 3

4 / 50

4. 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

5 / 50

5. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

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

d. Determine Possible therapeutic uses, Effective doses range

6 / 50

6. Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule Q

d. Schedule B

7 / 50

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

a. 500 patients

b. 1-10 patients

c. 10-12 patients

d. 100 patients

8 / 50

8. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase V

d. Phase III

9 / 50

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

a. Blue

b. Yellow

c. Red

d. White

10 / 50

10. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. Australia

d. India

11 / 50

11. 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. Chief Administrator medical officer of state

d. Government Analyst

12 / 50

12. 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

13 / 50

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

a. All

b. Chief pharmacist of government hospital

c. Assistant drug controller

d. Chief administrative medical officer of the state

14 / 50

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

a. 20

b. 21

c. 20B

d. 21B

15 / 50

15. MHRA is regulatory agency of ……….....

a. Denmark

b. UK

c. Brazil

d. South Africa

16 / 50

16. 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. Misbranded Drug

b. True Drug

c. Spurious Drug

d. Adulterated Drug

17 / 50

17. 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

18 / 50

18. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1948

c. 1919

d. 1985

19 / 50

19. 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 manufacture of Medical device

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

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

20 / 50

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

a. At temperature which not exceed 20°C

b. At temperature which not exceed 5°C

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

d. In cold place

21 / 50

21. 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

22 / 50

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

a. Temperature not exceeding 5°C

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

c. A cool place

d. A Cold place

23 / 50

23. Schedule J is related to

a. Pack sizes of drugs.

b. Curable disease

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

d. GMP

24 / 50

24. 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 F

b. Schedule Y

c. Schedule O

d. Schedule M

25 / 50

25. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule Q

d. Schedule O

26 / 50

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

a. 400 square meters

b. 150 square meters

c. 250 square meters

d. 500 square meters

27 / 50

27. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. X

d. C and C1

28 / 50

28. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule H

d. Schedule G

29 / 50

29. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule P1

30 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 6 year

d. Every 2 year

31 / 50

31. Patent Act is established in

a. 1940

b. 1948

c. 1919

d. 1970

32 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

33 / 50

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

a. 1940

b. 1955

c. 1985

d. 1950

34 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule O

d. Schedule R

35 / 50

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

a. Eight

b. Five

c. Four

d. Six

36 / 50

36. Hatch Waxman Act is related to

a. Banned drugs

b. Dangerous drugs Act

c. Over the counter drugs

d. Spurious drugs Act

37 / 50

37. 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 H

c. Schedule I

d. Schedule G

38 / 50

38. Example of Schedule G drug is

a. Barbital

b. Cefuroxime

c. Enalapril

d. Metformin

39 / 50

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

a. List of maximum equipments for efficiently running pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. Area required to open wholesale drug store

40 / 50

40. 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. G

d. H

41 / 50

41. Coca, opium and hemp come under:

a. Insecticide Act

b. Spurious Drug Act

c. Dangerous Drug Act

d. Poisons Act

42 / 50

42. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

43 / 50

43. 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

44 / 50

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

a. D

b. FF

c. Q

d. A

45 / 50

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

a. Five

b. Seven

c. Six

d. Nine

46 / 50

46. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

47 / 50

47. Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

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

d. List of minimum equipment for efficient running of pharmacy

48 / 50

48. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 25

c. Form 27

d. Form 24

49 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Misbranded drugs

d. Ayurvedic drugs

50 / 50

50. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule J

c. Schedule K

d. Schedule L

Your score is

The average score is 37%