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. Aspirin sodium comes under

a. Schedule H

b. Schedule J

c. Schedule G

d. Schedule Y

2 / 50

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

a. 1950

b. 1955

c. 1940

d. 1985

3 / 50

3. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

4 / 50

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

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

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

c. Requirements of factory premises

d. List of prescription drugs

5 / 50

5. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase III

d. Phase V

6 / 50

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

7 / 50

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

a. R1

b. S

c. R

d. O

8 / 50

8. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

9 / 50

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

a. 4

b. 3

c. 1

d. 2

10 / 50

10. Schedule J is related to

a. Curable disease

b. GMP

c. Pack sizes of drugs.

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

11 / 50

11. Dettol comes under

a. Schedule O

b. Schedule Q

c. Schedule P

d. Schedule N

12 / 50

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

a. President of India

b. Government Analyst

c. Chief Administrator medical officer of state

d. The officer in charge of drugs control organization

13 / 50

13. 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

14 / 50

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

a. Ayurvedic drugs

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Toilet preparations

15 / 50

15. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Spurious drugs Act

d. Banned drugs

16 / 50

16. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Homeopathy product

d. List of Ayurvedic product

17 / 50

17. Biological and Biotechnological products are included in schedule.

a. B

b. A

c. C and C1

d. X

18 / 50

18. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule P1

d. Schedule O

19 / 50

19. 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 J

c. Schedule H

d. Schedule G

20 / 50

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

a. Denmark

b. UK

c. Brazil

d. South Africa

21 / 50

21. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

22 / 50

22. Purpose of Phase-3 trial is

a. Long time adverse effects aster marketing drug

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

c. Determine Possible therapeutic uses, Effective doses range

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

23 / 50

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

a. 500 patients

b. 100 patients

c. 10-12 patients

d. 1-10 patients

24 / 50

24. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Enalapril

d. Cefuroxime

25 / 50

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

a. President, Pharmacy Council of India

b. Ministry of Education

c. Central Government

d. Drug Controller

26 / 50

26. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

27 / 50

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

a. Symbol X given in red

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

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

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

28 / 50

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

a. 400 square meters

b. 500 square meters

c. 250 square meters

d. 150 square meters

29 / 50

29. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

30 / 50

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

a. Schedule O

b. Schedule Q

c. Schedule R

d. Schedule P

31 / 50

31. MCC is regulatory agency of ……………

a. UK

b. Denmark

c. Brazil

d. South Africa

32 / 50

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

a. At temperature which not exceed 5°C

b. At temperature which not exceed 20°C

c. In cold place

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

33 / 50

33. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. Zimbabwe

d. India

34 / 50

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

a. Five

b. Nine

c. Seven

d. Six

35 / 50

35. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule K

d. Schedule J

36 / 50

36. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. Guidelines for clinical Trials

c. None of the above

d. List of generic drugs

37 / 50

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

a. H

b. K

c. X

d. G

38 / 50

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

a. Five

b. Eight

c. Four

d. Six

39 / 50

39. 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. W

d. V

40 / 50

40. Patent Act is established in

a. 1948

b. 1940

c. 1919

d. 1970

41 / 50

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

a. 20B

b. 21B

c. 21

d. 20

42 / 50

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

a. All

b. Chief administrative medical officer of the state

c. Assistant drug controller

d. Chief pharmacist of government hospital

43 / 50

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

a. Every 3 year

b. Every 6 year

c. Every 2 year

d. Every 5 year

44 / 50

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

a. Yellow

b. White

c. Blue

d. Red

45 / 50

45. 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. Misbranded Drug

c. Spurious Drug

d. Adulterated Drug

46 / 50

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

a. Parenteral preparation

b. Ophthalmic preparation

c. Skin cosmetic preparation

d. Ointment formulation

47 / 50

47. 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 Ayurveda, Sidhha and Unani drugs

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

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

48 / 50

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

a. A

b. Q

c. D

d. FF

49 / 50

49. 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

50 / 50

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

a. A cool place

b. Temperature not exceeding 5°C

c. A Cold place

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

Your score is

The average score is 38%