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. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Requirement of factory premises and hygienic condition to complied

c. Standard for cosmetics

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

2 / 50

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

a. In cold place

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. At temperature which not exceed 20°C

3 / 50

3. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule A

c. Schedule P

d. Schedule B

4 / 50

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

a. H

b. X

c. G

d. K

5 / 50

5. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1985

d. 1919

6 / 50

6. Patent Act is established in

a. 1970

b. 1919

c. 1948

d. 1940

7 / 50

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. President of India

d. Government Analyst

8 / 50

8. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

9 / 50

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

a. R

b. R1

c. O

d. S

10 / 50

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

a. Ointment formulation

b. Ophthalmic preparation

c. Parenteral preparation

d. Skin cosmetic preparation

11 / 50

11. Schedule C is related to

a. List of Biological and Immunological product

b. List of Allopathic product

c. List of Ayurvedic product

d. List of Homeopathy product

12 / 50

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

a. 1940

b. 1950

c. 1955

d. 1985

13 / 50

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

a. FF

b. Q

c. D

d. A

14 / 50

14. Example of Schedule G drug is

a. Metformin

b. Cefuroxime

c. Enalapril

d. Barbital

15 / 50

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

a. List of prescription drugs

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

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

d. Requirements of factory premises

16 / 50

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

a. Every 5 year

b. Every 2 year

c. Every 3 year

d. Every 6 year

17 / 50

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

a. 21

b. 21B

c. 20B

d. 20

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

a. Seven

b. Six

c. Nine

d. Five

20 / 50

20. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Denmark

d. Brazil

21 / 50

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

a. 1-10 patients

b. 500 patients

c. 10-12 patients

d. 100 patients

22 / 50

22. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule O

d. Schedule P

23 / 50

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

a. Chief administrative medical officer of the state

b. All

c. Chief pharmacist of government hospital

d. Assistant drug controller

24 / 50

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

a. Temperature not exceeding 5°C

b. A cool place

c. A Cold place

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

25 / 50

25. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule J

d. Schedule G

26 / 50

26. 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 G

c. Schedule J

d. Schedule H

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. Misbranded Drug

b. Adulterated Drug

c. Spurious Drug

d. True Drug

28 / 50

28. MCC is regulatory agency of ……………

a. Denmark

b. UK

c. Brazil

d. South Africa

29 / 50

29. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 26

d. Form 27

30 / 50

30. 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 manufacturer of Ayurveda, Sidhha and Unani drugs

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

31 / 50

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

a. Schedule R

b. Schedule P

c. Schedule Q

d. Schedule O

32 / 50

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

a. Six

b. Four

c. Five

d. Eight

33 / 50

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

a. Red

b. Blue

c. White

d. Yellow

34 / 50

34. 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 O

d. Schedule M

35 / 50

35. Coca, opium and hemp come under:

a. Insecticide Act

b. Poisons Act

c. Dangerous Drug Act

d. Spurious Drug Act

36 / 50

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

a. Central Government

b. Drug Controller

c. President, Pharmacy Council of India

d. Ministry of Education

37 / 50

37. 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. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

38 / 50

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

a. X

b. Y

c. V

d. W

39 / 50

39. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

40 / 50

40. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule K

d. Schedule P

41 / 50

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

a. 150 square meters

b. 500 square meters

c. 250 square meters

d. 400 square meters

42 / 50

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

a. 4

b. 3

c. 2

d. 1

43 / 50

43. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. C and C1

d. X

44 / 50

44. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

45 / 50

45. Schedule J is related to

a. Curable disease

b. Pack sizes of drugs.

c. GMP

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

46 / 50

46. TGA is regulatory agency of………….

a. Australia

b. Denmark

c. Zimbabwe

d. India

47 / 50

47. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Over the counter drugs

d. Banned drugs

48 / 50

48. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

49 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Misbranded drugs

c. Toilet preparations

d. Ayurvedic drugs

50 / 50

50. 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

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The average score is 38%