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

a. Schedule H

b. Schedule J

c. Schedule G

d. Schedule I

2 / 50

2. 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

3 / 50

3. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Cefuroxime

d. Enalapril

4 / 50

4. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

5 / 50

5. 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 cool place

c. Temperature not exceeding 5°C

d. A Cold place

6 / 50

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

a. Parenteral preparation

b. Ointment formulation

c. Skin cosmetic preparation

d. Ophthalmic preparation

7 / 50

7. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

8 / 50

8. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1954

c. 1985

d. 1948

9 / 50

9. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. B

d. A

10 / 50

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

a. Area required to open wholesale drug store

b. List of maximum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. List of minimum equipments for efficiently running pharmacy

11 / 50

11. 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

12 / 50

12. 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. Adulterated Drug

b. Misbranded Drug

c. Spurious Drug

d. True Drug

13 / 50

13. TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. India

d. Denmark

14 / 50

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

a. At temperature which not exceed 20°C

b. In cold place

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

d. At temperature which not exceed 5°C

15 / 50

15. Dettol comes under

a. Schedule Q

b. Schedule P

c. Schedule N

d. Schedule O

16 / 50

16. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Dangerous Drug Act

c. Insecticide Act

d. Poisons Act

17 / 50

17. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule Q

d. Schedule P

18 / 50

18. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

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

d. Long time adverse effects aster marketing drug

19 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule R

d. Schedule O

20 / 50

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

a. Red

b. Yellow

c. Blue

d. White

21 / 50

21. Aspirin sodium comes under

a. Schedule J

b. Schedule Y

c. Schedule G

d. Schedule H

22 / 50

22. Schedule C is related to

a. List of Homeopathy product

b. List of Allopathic product

c. List of Biological and Immunological product

d. List of Ayurvedic product

23 / 50

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

a. Government Analyst

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. President of India

24 / 50

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

a. 1950

b. 1955

c. 1985

d. 1940

25 / 50

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

a. 100 patients

b. 500 patients

c. 10-12 patients

d. 1-10 patients

26 / 50

26. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule L

d. Schedule K

27 / 50

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

a. X

b. G

c. K

d. H

28 / 50

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

a. Six

b. Four

c. Five

d. Eight

29 / 50

29. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

30 / 50

30. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Poisonous Act.

c. Drug and magic Remedies Act

d. The Medical Termination of pregnancy Act

31 / 50

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

a. Seven

b. Five

c. Nine

d. Six

32 / 50

32. Schedule J is related to

a. Curable disease

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

c. Pack sizes of drugs.

d. GMP

33 / 50

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

a. X

b. W

c. Y

d. V

34 / 50

34. 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

35 / 50

35. 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

36 / 50

36. 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. List of prescription drugs

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

d. Requirements of factory premises

37 / 50

37. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. None of the above

c. List of generic drugs

d. Guidelines for clinical Trials

38 / 50

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

a. 3

b. 1

c. 2

d. 4

39 / 50

39. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

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

d. List of minimum equipment for efficient running of pharmacy

40 / 50

40. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

41 / 50

41. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase V

d. Phase III

42 / 50

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

a. Every 2 year

b. Every 3 year

c. Every 6 year

d. Every 5 year

43 / 50

43. For schedule X drug use of Human beings special labeling requirement require is

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

b. Symbol X given in red

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

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

44 / 50

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

a. 500 square meters

b. 250 square meters

c. 400 square meters

d. 150 square meters

45 / 50

45. Pack size of drug is covered under

a. Schedule O

b. Schedule P1

c. Schedule R

d. Schedule P

46 / 50

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

a. S

b. R1

c. O

d. R

47 / 50

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

a. Toilet preparations

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

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

a. A

b. FF

c. D

d. Q

50 / 50

50. Patent Act is established in

a. 1940

b. 1948

c. 1919

d. 1970

Your score is

The average score is 38%