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. Which of the following is prohibited to be imported?

a. Toilet preparations

b. Misbranded drugs

c. Ayurvedic drugs

d. Schedule ‘C’ ‘G’ drugs

2 / 50

2. Patent Act is established in

a. 1919

b. 1970

c. 1948

d. 1940

3 / 50

3. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase II

d. Phase V

4 / 50

4. 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

5 / 50

5. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. UK

d. Brazil

6 / 50

6. Example of Schedule G drug is

a. Barbital

b. Enalapril

c. Metformin

d. Cefuroxime

7 / 50

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

a. Chief Administrator medical officer of state

b. The officer in charge of drugs control organization

c. Government Analyst

d. President of India

8 / 50

8. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

9 / 50

9. 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

10 / 50

10. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. Standard for cosmetics

c. List of minimum equipment for efficient running of pharmacy

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

11 / 50

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

a. D

b. A

c. Q

d. FF

12 / 50

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

a. Nine

b. Six

c. Five

d. Seven

13 / 50

13. 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

14 / 50

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

a. 500 patients

b. 10-12 patients

c. 1-10 patients

d. 100 patients

15 / 50

15. 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. X

d. G

16 / 50

16. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Banned drugs

c. Over the counter drugs

d. Dangerous drugs Act

17 / 50

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

a. 2

b. 3

c. 4

d. 1

18 / 50

18. 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

19 / 50

19. 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

20 / 50

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

a. 500 square meters

b. 250 square meters

c. 150 square meters

d. 400 square meters

21 / 50

21. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. B

d. X

22 / 50

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

a. Red

b. White

c. Yellow

d. Blue

23 / 50

23. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 27

c. Form 26

d. Form 24

24 / 50

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

a. Drug Controller

b. Ministry of Education

c. President, Pharmacy Council of India

d. Central Government

25 / 50

25. MHRA is regulatory agency of ……….....

a. South Africa

b. UK

c. Brazil

d. Denmark

26 / 50

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

a. Four

b. Six

c. Eight

d. Five

27 / 50

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

a. Schedule O

b. Schedule P

c. Schedule R

d. Schedule Q

28 / 50

28. Schedule J is related to

a. GMP

b. Pack sizes of drugs.

c. Curable disease

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

29 / 50

29. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule K

d. Schedule P

30 / 50

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

a. O

b. S

c. R1

d. R

31 / 50

31. Aspirin sodium comes under

a. Schedule Y

b. Schedule J

c. Schedule H

d. Schedule G

32 / 50

32. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. India

d. Zimbabwe

33 / 50

33. 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 F

b. Schedule M

c. Schedule O

d. Schedule Y

34 / 50

34. Dettol comes under

a. Schedule P

b. Schedule Q

c. Schedule O

d. Schedule N

35 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

36 / 50

36. Coca, opium and hemp come under:

a. Poisons Act

b. Insecticide Act

c. Spurious Drug Act

d. Dangerous Drug Act

37 / 50

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

a. Chief pharmacist of government hospital

b. Assistant drug controller

c. Chief administrative medical officer of the state

d. All

38 / 50

38. 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 H

c. Schedule G

d. Schedule J

39 / 50

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

a. List of prescription drugs

b. Requirements of factory premises

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

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

40 / 50

40. 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. Temperature not exceeding 5°C

c. A Cold place

d. A cool place

41 / 50

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

42 / 50

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

a. 21

b. 20B

c. 20

d. 21B

43 / 50

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

a. Every 2 year

b. Every 5 year

c. Every 6 year

d. Every 3 year

44 / 50

44. Pack size of drug is covered under

a. Schedule R

b. Schedule O

c. Schedule P

d. Schedule P1

45 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

46 / 50

46. 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

47 / 50

47. 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. Spurious Drug

c. Adulterated Drug

d. True Drug

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. X

b. Y

c. V

d. W

49 / 50

49. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. List of incurable diseases

d. None of the above

50 / 50

50. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

Your score is

The average score is 37%