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

365

1 / 50

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

a. Five

b. Nine

c. Six

d. Seven

2 / 50

2. 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

3 / 50

3. 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.

4 / 50

4. 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. 21B

d. 20

5 / 50

5. Schedule J is related to

a. Curable disease

b. GMP

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

d. Pack sizes of drugs.

6 / 50

6. 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 M

c. Schedule F

d. Schedule O

7 / 50

7. Patent Act is established in

a. 1970

b. 1940

c. 1919

d. 1948

8 / 50

8. 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

9 / 50

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

a. Area for opening retail pharmacy

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area required to open wholesale drug store

10 / 50

10. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

11 / 50

11. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule O

d. Schedule N

12 / 50

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

a. 250 square meters

b. 500 square meters

c. 400 square meters

d. 150 square meters

13 / 50

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

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

b. A Cold place

c. Temperature not exceeding 5°C

d. A cool place

14 / 50

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

a. 1

b. 3

c. 2

d. 4

15 / 50

15. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1948

c. 1919

d. 1954

16 / 50

16. 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

17 / 50

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

a. President of India

b. The officer in charge of drugs control organization

c. Government Analyst

d. Chief Administrator medical officer of state

18 / 50

18. Biological and Biotechnological products are included in schedule.

a. B

b. C and C1

c. A

d. X

19 / 50

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

a. 1955

b. 1950

c. 1940

d. 1985

20 / 50

20. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. List of minimum equipment for efficient running of pharmacy

d. Standard for cosmetics

21 / 50

21. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

22 / 50

22. 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 H displayed on right top corner of the label.

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

23 / 50

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

a. Every 6 year

b. Every 3 year

c. Every 5 year

d. Every 2 year

24 / 50

24. 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. Spurious Drug

d. True Drug

25 / 50

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

a. South Africa

b. Brazil

c. UK

d. Denmark

26 / 50

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

a. R

b. R1

c. O

d. S

27 / 50

27. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

28 / 50

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

a. Eight

b. Six

c. Four

d. Five

29 / 50

29. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

30 / 50

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

a. Yellow

b. Red

c. White

d. Blue

31 / 50

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

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

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 manufacture of Medical device

32 / 50

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

a. 100 patients

b. 10-12 patients

c. 500 patients

d. 1-10 patients

33 / 50

33. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

34 / 50

34. TGA is regulatory agency of………….

a. India

b. Denmark

c. Zimbabwe

d. Australia

35 / 50

35. Purpose of Phase-3 trial is

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

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

c. Determine Possible therapeutic uses, Effective doses range

d. Long time adverse effects aster marketing drug

36 / 50

36. 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 H

c. Schedule I

d. Schedule J

37 / 50

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

a. Chief pharmacist of government hospital

b. All

c. Assistant drug controller

d. Chief administrative medical officer of the state

38 / 50

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

a. List of prescription drugs

b. Requirements of factory premises

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

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

39 / 50

39. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 26

d. Form 27

40 / 50

40. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Ayurvedic product

d. List of Homeopathy product

41 / 50

41. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Metformin

d. Barbital

42 / 50

42. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

43 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Toilet preparations

d. Misbranded drugs

44 / 50

44. 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 5°C

c. At temperature which not exceed 20°C

d. In cold place

45 / 50

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

a. Central Government

b. Ministry of Education

c. President, Pharmacy Council of India

d. Drug Controller

46 / 50

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

a. D

b. FF

c. Q

d. A

47 / 50

47. Injection syringe and needles are covered under

a. Schedule B

b. Schedule A

c. Schedule P

d. Schedule Q

48 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

49 / 50

49. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. None of the above

d. List of incurable diseases

50 / 50

50. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase I

c. Phase II

d. Phase III

Your score is

The average score is 38%