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. Patent Act is established in

a. 1919

b. 1970

c. 1948

d. 1940

2 / 50

2. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule J

d. Schedule G

3 / 50

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

a. White

b. Blue

c. Red

d. Yellow

4 / 50

4. 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

5 / 50

5. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

6 / 50

6. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Barbital

d. Cefuroxime

7 / 50

7. 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

8 / 50

8. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

b. Determine Possible therapeutic uses, Effective doses range

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)

9 / 50

9. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

10 / 50

10. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule O

d. Schedule R

11 / 50

11. 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. X

d. K

12 / 50

12. 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 O

c. Schedule Y

d. Schedule M

13 / 50

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

a. Nine

b. Seven

c. Six

d. Five

14 / 50

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

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

b. Requirements of factory premises

c. List of prescription drugs

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

15 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Central Government

d. Drug Controller

16 / 50

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

a. Government Analyst

b. President of India

c. The officer in charge of drugs control organization

d. Chief Administrator medical officer of state

17 / 50

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

a. 500 square meters

b. 400 square meters

c. 250 square meters

d. 150 square meters

18 / 50

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

a. R1

b. O

c. R

d. S

19 / 50

19. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

20 / 50

20. 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

21 / 50

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

a. 1955

b. 1950

c. 1940

d. 1985

22 / 50

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

a. Eight

b. Five

c. Six

d. Four

23 / 50

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

a. D

b. Q

c. A

d. FF

24 / 50

24. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule Q

d. Schedule P

25 / 50

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

a. Misbranded drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

26 / 50

26. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 24

d. Form 25

27 / 50

27. 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

28 / 50

28. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

29 / 50

29. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Over the counter drugs

d. Spurious drugs Act

30 / 50

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

a. 1

b. 2

c. 4

d. 3

31 / 50

31. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule N

32 / 50

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

a. 20

b. 21B

c. 20B

d. 21

33 / 50

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

a. 100 patients

b. 10-12 patients

c. 1-10 patients

d. 500 patients

34 / 50

34. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule K

d. Schedule J

35 / 50

35. 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

36 / 50

36. TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. India

d. Denmark

37 / 50

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

a. Schedule O

b. Schedule P

c. Schedule R

d. Schedule Q

38 / 50

38. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. A

d. B

39 / 50

39. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

40 / 50

40. 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

41 / 50

41. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. Guidelines for clinical Trials

d. List of incurable diseases

42 / 50

42. 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

43 / 50

43. 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. In cold place

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

44 / 50

44. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Allopathic product

d. List of Biological and Immunological product

45 / 50

45. MHRA is regulatory agency of ……….....

a. Denmark

b. UK

c. South Africa

d. Brazil

46 / 50

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

a. Chief administrative medical officer of the state

b. Assistant drug controller

c. All

d. Chief pharmacist of government hospital

47 / 50

47. 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. X

d. W

48 / 50

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

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

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

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

49 / 50

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

a. Every 2 year

b. Every 5 year

c. Every 6 year

d. Every 3 year

50 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Parenteral preparation

d. Ointment formulation

Your score is

The average score is 37%