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. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. A

d. B

2 / 50

2. 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

3 / 50

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

a. Requirements of factory premises

b. List of prescription drugs

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

4 / 50

4. TGA is regulatory agency of………….

a. Denmark

b. India

c. Zimbabwe

d. Australia

5 / 50

5. 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. List of minimum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

6 / 50

6. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule J

d. Schedule G

7 / 50

7. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule L

c. Schedule P

d. Schedule J

8 / 50

8. Schedule J is related to

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

b. Curable disease

c. Pack sizes of drugs.

d. GMP

9 / 50

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

10 / 50

10. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Poisonous Act.

d. Narcotic and psychotropic substance Act

11 / 50

11. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

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. True Drug

d. Spurious Drug

13 / 50

13. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase I

c. Phase III

d. Phase V

14 / 50

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

a. Schedule Q

b. Schedule R

c. Schedule P

d. Schedule O

15 / 50

15. 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 20°C

c. In cold place

d. At temperature which not exceed 5°C

16 / 50

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

a. Eight

b. Four

c. Six

d. Five

17 / 50

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

a. Government Analyst

b. Chief Administrator medical officer of state

c. President of India

d. The officer in charge of drugs control organization

18 / 50

18. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule B

c. Schedule A

d. Schedule P

19 / 50

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

a. 3

b. 1

c. 4

d. 2

20 / 50

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

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

21 / 50

21. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1985

c. 1954

d. 1919

22 / 50

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

a. FF

b. D

c. A

d. Q

23 / 50

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Ointment formulation

24 / 50

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

a. 100 patients

b. 500 patients

c. 1-10 patients

d. 10-12 patients

25 / 50

25. Schedule C is related to

a. List of Homeopathy product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Allopathic product

26 / 50

26. Dettol comes under

a. Schedule N

b. Schedule Q

c. Schedule P

d. Schedule O

27 / 50

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

a. Six

b. Seven

c. Five

d. Nine

28 / 50

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

a. Every 3 year

b. Every 2 year

c. Every 6 year

d. Every 5 year

29 / 50

29. Example of Schedule G drug is

a. Enalapril

b. Cefuroxime

c. Metformin

d. Barbital

30 / 50

30. 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 F

d. Schedule O

31 / 50

31. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

c. Long time adverse effects aster marketing drug

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

32 / 50

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

a. All

b. Assistant drug controller

c. Chief administrative medical officer of the state

d. Chief pharmacist of government hospital

33 / 50

33. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. List of incurable diseases

d. Guidelines for clinical Trials

34 / 50

34. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Insecticide Act

c. Poisons Act

d. Dangerous Drug Act

35 / 50

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

a. Toilet preparations

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Ayurvedic drugs

36 / 50

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

a. W

b. X

c. Y

d. V

37 / 50

37. 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 I

d. Schedule G

38 / 50

38. 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 manufacture of Medical device

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

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

39 / 50

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

a. O

b. R

c. R1

d. S

40 / 50

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

a. Drug Controller

b. President, Pharmacy Council of India

c. Ministry of Education

d. Central Government

41 / 50

41. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule R

d. Schedule P

42 / 50

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

a. Yellow

b. White

c. Red

d. Blue

43 / 50

43. MCC is regulatory agency of ……………

a. Brazil

b. South Africa

c. UK

d. Denmark

44 / 50

44. MHRA is regulatory agency of ……….....

a. South Africa

b. Denmark

c. Brazil

d. UK

45 / 50

45. Patent Act is established in

a. 1940

b. 1919

c. 1948

d. 1970

46 / 50

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

a. K

b. H

c. G

d. X

47 / 50

47. 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

48 / 50

48. Hatch Waxman Act is related to

a. Banned drugs

b. Spurious drugs Act

c. Over the counter drugs

d. Dangerous drugs Act

49 / 50

49. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

b. Standard for cosmetics

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

d. Requirement of factory premises and hygienic condition to complied

50 / 50

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

a. 1985

b. 1950

c. 1955

d. 1940

Your score is

The average score is 37%