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

295

1 / 50

1. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1985

c. 1954

d. 1948

2 / 50

2. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. South Africa

d. Denmark

3 / 50

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

a. Four

b. Five

c. Eight

d. Six

4 / 50

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

a. 10-12 patients

b. 1-10 patients

c. 100 patients

d. 500 patients

5 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

6 / 50

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

a. Central Government

b. Ministry of Education

c. President, Pharmacy Council of India

d. Drug Controller

7 / 50

7. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

8 / 50

8. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Poisons Act

d. Spurious Drug Act

9 / 50

9. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Over the counter drugs

c. Banned drugs

d. Spurious drugs Act

10 / 50

10. 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 manufacturer of Homeopathy drugs

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

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

11 / 50

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

a. Red

b. Yellow

c. White

d. Blue

12 / 50

12. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule P

c. Schedule L

d. Schedule K

13 / 50

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

a. 21B

b. 21

c. 20

d. 20B

14 / 50

14. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Poisonous Act.

c. Drug and magic Remedies Act

d. Narcotic and psychotropic substance Act

15 / 50

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

a. 2

b. 3

c. 4

d. 1

16 / 50

16. Schedule N states

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

b. Standard for cosmetics

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

17 / 50

17. Post marketing surveillance comes under clinical trial

a. Phase II

b. Phase III

c. Phase V

d. Phase I

18 / 50

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

a. FF

b. Q

c. A

d. D

19 / 50

19. 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. Requirements of factory premises

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

20 / 50

20. Patent Act is established in

a. 1940

b. 1919

c. 1970

d. 1948

21 / 50

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

a. 1940

b. 1955

c. 1950

d. 1985

22 / 50

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

a. W

b. V

c. X

d. Y

23 / 50

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

a. Chief pharmacist of government hospital

b. Chief administrative medical officer of the state

c. All

d. Assistant drug controller

24 / 50

24. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule P1

d. Schedule O

25 / 50

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

a. G

b. X

c. K

d. H

26 / 50

26. Injection syringe and needles are covered under

a. Schedule Q

b. Schedule P

c. Schedule B

d. Schedule A

27 / 50

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

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

d. Symbol X given in red

28 / 50

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

a. Every 3 year

b. Every 5 year

c. Every 2 year

d. Every 6 year

29 / 50

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. Government Analyst

d. President of India

30 / 50

30. 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. Spurious Drug

c. Misbranded Drug

d. Adulterated Drug

31 / 50

31. 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

32 / 50

32. Schedule J is related to

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

b. Curable disease

c. GMP

d. Pack sizes of drugs.

33 / 50

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

a. A cool place

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

c. Temperature not exceeding 5°C

d. A Cold place

34 / 50

34. 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

35 / 50

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

a. Ayurvedic drugs

b. Toilet preparations

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

36 / 50

36. Example of Schedule G drug is

a. Cefuroxime

b. Enalapril

c. Metformin

d. Barbital

37 / 50

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

a. R1

b. O

c. S

d. R

38 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area required to open wholesale drug store

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

39 / 50

39. MCC is regulatory agency of ……………

a. South Africa

b. Denmark

c. UK

d. Brazil

40 / 50

40. Dettol comes under

a. Schedule O

b. Schedule N

c. Schedule P

d. Schedule Q

41 / 50

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

a. Seven

b. Six

c. Five

d. Nine

42 / 50

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

a. 150 square meters

b. 400 square meters

c. 500 square meters

d. 250 square meters

43 / 50

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

a. Schedule R

b. Schedule O

c. Schedule Q

d. Schedule P

44 / 50

44. 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 I

d. Schedule H

45 / 50

45. Biological and Biotechnological products are included in schedule.

a. X

b. A

c. C and C1

d. B

46 / 50

46. 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 Y

c. Schedule M

d. Schedule O

47 / 50

47. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 26

c. Form 24

d. Form 27

48 / 50

48. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule J

d. Schedule Y

49 / 50

49. TGA is regulatory agency of………….

a. Zimbabwe

b. India

c. Denmark

d. Australia

50 / 50

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

a. In cold place

b. At temperature which not exceed 5°C

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

d. At temperature which not exceed 20°C

Your score is

The average score is 36%