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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

2 / 50

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

a. 3

b. 1

c. 4

d. 2

3 / 50

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

a. Central Government

b. Drug Controller

c. Ministry of Education

d. President, Pharmacy Council of India

4 / 50

4. Coca, opium and hemp come under:

a. Poisons Act

b. Insecticide Act

c. Spurious Drug Act

d. Dangerous Drug Act

5 / 50

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

a. Temperature not exceeding 5°C

b. A Cold place

c. A cool place

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

6 / 50

6. 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. Spurious Drug

b. Misbranded Drug

c. True Drug

d. Adulterated Drug

7 / 50

7. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. The Medical Termination of pregnancy Act

d. Poisonous Act.

8 / 50

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

9 / 50

9. 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)

10 / 50

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

a. Schedule P

b. Schedule R

c. Schedule Q

d. Schedule O

11 / 50

11. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule P

d. Schedule Q

12 / 50

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

a. 20B

b. 21

c. 20

d. 21B

13 / 50

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

a. White

b. Yellow

c. Red

d. Blue

14 / 50

14. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. South Africa

d. Brazil

15 / 50

15. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

16 / 50

16. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule P

d. Schedule R

17 / 50

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

a. 1985

b. 1955

c. 1940

d. 1950

18 / 50

18. 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

19 / 50

19. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Dangerous drugs Act

d. Spurious drugs Act

20 / 50

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

a. 1-10 patients

b. 100 patients

c. 10-12 patients

d. 500 patients

21 / 50

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

a. Nine

b. Five

c. Seven

d. Six

22 / 50

22. Patent Act is established in

a. 1970

b. 1940

c. 1948

d. 1919

23 / 50

23. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule J

c. Schedule P

d. Schedule K

24 / 50

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

a. In cold place

b. At temperature which not exceed 20°C

c. At temperature which not exceed 5°C

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

25 / 50

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

a. Four

b. Six

c. Five

d. Eight

26 / 50

26. 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 X given in red

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

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

27 / 50

27. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1919

d. 1954

28 / 50

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

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

29 / 50

29. 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

30 / 50

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

31 / 50

31. 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

32 / 50

32. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. A

d. C and C1

33 / 50

33. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

34 / 50

34. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Brazil

d. Denmark

35 / 50

35. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

36 / 50

36. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase II

c. Phase I

d. Phase V

37 / 50

37. Injection syringe and needles are covered under

a. Schedule B

b. Schedule Q

c. Schedule P

d. Schedule A

38 / 50

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

a. Schedule G

b. Schedule I

c. Schedule J

d. Schedule H

39 / 50

39. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule Y

d. Schedule G

40 / 50

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

a. G

b. K

c. X

d. H

41 / 50

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

a. D

b. A

c. FF

d. Q

42 / 50

42. 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

43 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Ayurvedic drugs

d. Toilet preparations

44 / 50

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

a. 150 square meters

b. 250 square meters

c. 400 square meters

d. 500 square meters

45 / 50

45. 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. Chief pharmacist of government hospital

d. All

46 / 50

46. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 27

d. Form 24

47 / 50

47. Schedule J is related to

a. Pack sizes of drugs.

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

c. Curable disease

d. GMP

48 / 50

48. 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

49 / 50

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

a. S

b. R

c. O

d. R1

50 / 50

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

a. President of India

b. Chief Administrator medical officer of state

c. The officer in charge of drugs control organization

d. Government Analyst

Your score is

The average score is 37%