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

336

1 / 50

1. TGA is regulatory agency of………….

a. India

b. Denmark

c. Australia

d. Zimbabwe

2 / 50

2. 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 manufacture of Medical device

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

3 / 50

3. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

c. Long time adverse effects aster marketing drug

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

4 / 50

4. 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 Y

c. Schedule O

d. Schedule F

5 / 50

5. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule N

d. Schedule P

6 / 50

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

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

b. List of prescription drugs

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

d. Requirements of factory premises

7 / 50

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

a. Yellow

b. White

c. Blue

d. Red

8 / 50

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

a. FF

b. A

c. D

d. Q

9 / 50

9. Patent Act is established in

a. 1970

b. 1948

c. 1940

d. 1919

10 / 50

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

a. 1955

b. 1950

c. 1940

d. 1985

11 / 50

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

a. Chief Administrator medical officer of state

b. Government Analyst

c. President of India

d. The officer in charge of drugs control organization

12 / 50

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

a. Drug Controller

b. Ministry of Education

c. President, Pharmacy Council of India

d. Central Government

13 / 50

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

a. At temperature which not exceed 20°C

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

c. At temperature which not exceed 5°C

d. In cold place

14 / 50

14. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule K

d. Schedule J

15 / 50

15. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Dangerous Drug Act

d. Poisons Act

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. 20

c. 20B

d. 21

17 / 50

17. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

18 / 50

18. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. X

d. C and C1

19 / 50

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

a. 10-12 patients

b. 500 patients

c. 100 patients

d. 1-10 patients

20 / 50

20. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

21 / 50

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

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule Q

22 / 50

22. Schedule J is related to

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

b. Pack sizes of drugs.

c. GMP

d. Curable disease

23 / 50

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

a. Misbranded drugs

b. Toilet preparations

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

24 / 50

24. MCC is regulatory agency of ……………

a. Denmark

b. UK

c. Brazil

d. South Africa

25 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

26 / 50

26. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. List of incurable diseases

d. None of the above

27 / 50

27. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

28 / 50

28. 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

29 / 50

29. 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

30 / 50

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

a. W

b. Y

c. X

d. V

31 / 50

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

a. S

b. O

c. R1

d. R

32 / 50

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

a. Five

b. Nine

c. Seven

d. Six

33 / 50

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

34 / 50

34. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

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

d. List of minimum equipment for efficient running of pharmacy

35 / 50

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

a. Ophthalmic preparation

b. Ointment formulation

c. Parenteral preparation

d. Skin cosmetic preparation

36 / 50

36. 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. Adulterated Drug

c. True Drug

d. Spurious Drug

37 / 50

37. Pack size of drug is covered under

a. Schedule O

b. Schedule R

c. Schedule P

d. Schedule P1

38 / 50

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

a. 2

b. 1

c. 3

d. 4

39 / 50

39. Aspirin sodium comes under

a. Schedule J

b. Schedule H

c. Schedule Y

d. Schedule G

40 / 50

40. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1985

d. 1954

41 / 50

41. Example of Schedule G drug is

a. Barbital

b. Metformin

c. Cefuroxime

d. Enalapril

42 / 50

42. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

43 / 50

43. For schedule X drug use of Human beings special labeling requirement require is

a. Symbol X given in red

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

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

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

44 / 50

44. MHRA is regulatory agency of ……….....

a. South Africa

b. Denmark

c. Brazil

d. UK

45 / 50

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

a. G

b. H

c. K

d. X

46 / 50

46. 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 J

c. Schedule H

d. Schedule G

47 / 50

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

a. Four

b. Eight

c. Six

d. Five

48 / 50

48. Hatch Waxman Act is related to

a. Over the counter drugs

b. Spurious drugs Act

c. Banned drugs

d. Dangerous drugs Act

49 / 50

49. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

50 / 50

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

Your score is

The average score is 37%