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. Schedule N states

a. Standard for cosmetics

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

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

2 / 50

2. Injection syringe and needles are covered under

a. Schedule B

b. Schedule Q

c. Schedule A

d. Schedule P

3 / 50

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

a. Every 5 year

b. Every 6 year

c. Every 2 year

d. Every 3 year

4 / 50

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

a. A

b. Q

c. FF

d. D

5 / 50

5. Patent Act is established in

a. 1940

b. 1970

c. 1919

d. 1948

6 / 50

6. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. C and C1

d. X

7 / 50

7. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule N

d. Schedule O

8 / 50

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

a. 1955

b. 1985

c. 1950

d. 1940

9 / 50

9. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Denmark

d. Australia

10 / 50

10. 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

11 / 50

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

a. Central Government

b. President, Pharmacy Council of India

c. Ministry of Education

d. Drug Controller

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 M

b. Schedule Y

c. Schedule O

d. Schedule F

13 / 50

13. MCC is regulatory agency of ……………

a. Denmark

b. South Africa

c. UK

d. Brazil

14 / 50

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

a. In cold place

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. At temperature which not exceed 20°C

15 / 50

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

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule Q

16 / 50

16. 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 manufacture of Medical device

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

d. Requirements of factory premises for the manufacturer of Allopathy drugs

17 / 50

17. Example of Schedule G drug is

a. Metformin

b. Enalapril

c. Barbital

d. Cefuroxime

18 / 50

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

a. 1-10 patients

b. 10-12 patients

c. 100 patients

d. 500 patients

19 / 50

19. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Drug and magic Remedies Act

20 / 50

20. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1948

c. 1919

d. 1985

21 / 50

21. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

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

d. Determine Possible therapeutic uses, Effective doses range

22 / 50

22. 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. K

d. G

23 / 50

23. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Dangerous Drug Act

d. Poisons Act

24 / 50

24. Schedule C is related to

a. List of Allopathic product

b. List of Homeopathy product

c. List of Biological and Immunological product

d. List of Ayurvedic product

25 / 50

25. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Dangerous drugs Act

d. Over the counter drugs

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 H displayed on right top corner of the label.

c. Symbol X given in red

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

27 / 50

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

a. Seven

b. Six

c. Nine

d. Five

28 / 50

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

a. Skin cosmetic preparation

b. Parenteral preparation

c. Ophthalmic preparation

d. Ointment formulation

29 / 50

29. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule P1

d. Schedule O

30 / 50

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

a. Assistant drug controller

b. All

c. Chief pharmacist of government hospital

d. Chief administrative medical officer of the state

31 / 50

31. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. South Africa

d. UK

32 / 50

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

a. O

b. R1

c. R

d. S

33 / 50

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

a. 500 square meters

b. 150 square meters

c. 250 square meters

d. 400 square meters

34 / 50

34. Schedule J is related to

a. GMP

b. Curable disease

c. Pack sizes of drugs.

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

35 / 50

35. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule G

d. Schedule J

36 / 50

36. 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. Requirements of factory premises

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

37 / 50

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

a. Chief Administrator medical officer of state

b. President of India

c. Government Analyst

d. The officer in charge of drugs control organization

38 / 50

38. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase II

d. Phase III

39 / 50

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

a. Toilet preparations

b. Ayurvedic drugs

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

40 / 50

40. Schedule X of Drugs and Cosmetics Act comprises

a. None of the above

b. Guidelines for clinical Trials

c. List of generic drugs

d. List of incurable diseases

41 / 50

41. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

42 / 50

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

a. 3

b. 1

c. 4

d. 2

43 / 50

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

a. Red

b. Blue

c. White

d. Yellow

44 / 50

44. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 26

d. Form 24

45 / 50

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

a. 21B

b. 20B

c. 20

d. 21

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 J

b. Schedule G

c. Schedule H

d. Schedule I

47 / 50

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

a. Four

b. Eight

c. Six

d. Five

48 / 50

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

a. V

b. X

c. W

d. Y

49 / 50

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

a. Temperature not exceeding 5°C

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

c. A cool place

d. A Cold place

50 / 50

50. 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. Adulterated Drug

c. Spurious Drug

d. Misbranded Drug

Your score is

The average score is 37%