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

351

1 / 50

1. Dettol comes under

a. Schedule N

b. Schedule O

c. Schedule P

d. Schedule Q

2 / 50

2. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Cefuroxime

d. Enalapril

3 / 50

3. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Narcotic and psychotropic substance Act

c. Poisonous Act.

d. The Medical Termination of pregnancy Act

4 / 50

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

a. A cool place

b. Temperature not exceeding 5°C

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

d. A Cold place

5 / 50

5. 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

6 / 50

6. 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

7 / 50

7. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule J

d. Schedule K

8 / 50

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

a. All

b. Assistant drug controller

c. Chief pharmacist of government hospital

d. Chief administrative medical officer of the state

9 / 50

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

a. Red

b. White

c. Blue

d. Yellow

10 / 50

10. 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 F

c. Schedule O

d. Schedule M

11 / 50

11. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule Q

d. Schedule P

12 / 50

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

a. 2

b. 4

c. 1

d. 3

13 / 50

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

a. K

b. G

c. H

d. X

14 / 50

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

a. Central Government

b. Ministry of Education

c. Drug Controller

d. President, Pharmacy Council of India

15 / 50

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

a. Seven

b. Nine

c. Six

d. Five

16 / 50

16. 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

17 / 50

17. 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 I

c. Schedule G

d. Schedule J

18 / 50

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

a. 1940

b. 1955

c. 1950

d. 1985

19 / 50

19. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. Denmark

d. South Africa

20 / 50

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

a. UK

b. South Africa

c. Denmark

d. Brazil

21 / 50

21. Pack size of drug is covered under

a. Schedule P1

b. Schedule P

c. Schedule R

d. Schedule O

22 / 50

22. Schedule C is related to

a. List of Biological and Immunological product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Allopathic product

23 / 50

23. 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

24 / 50

24. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

25 / 50

25. Schedule J is related to

a. GMP

b. Pack sizes of drugs.

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

d. Curable disease

26 / 50

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

a. Four

b. Six

c. Five

d. Eight

27 / 50

27. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Poisons Act

c. Spurious Drug Act

d. Insecticide Act

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. Which of the following is prohibited to be imported?

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Misbranded drugs

d. Ayurvedic drugs

30 / 50

30. 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

31 / 50

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

a. 21

b. 20

c. 21B

d. 20B

32 / 50

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

a. The officer in charge of drugs control organization

b. Government Analyst

c. Chief Administrator medical officer of state

d. President of India

33 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. Area for opening retail pharmacy

c. Area required to open wholesale drug store

d. List of maximum equipments for efficiently running pharmacy

34 / 50

34. 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

35 / 50

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

a. V

b. Y

c. W

d. X

36 / 50

36. Schedule N states

a. Standard for cosmetics

b. List of minimum equipment for efficient running of pharmacy

c. Requirement of factory premises and hygienic condition to complied

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

37 / 50

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

a. List of prescription drugs

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

c. Requirements of factory premises

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

38 / 50

38. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Banned drugs

d. Over the counter drugs

39 / 50

39. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 26

c. Form 25

d. Form 24

40 / 50

40. Drug and Magic Remedies Act is enacted in

a. 1919

b. 1948

c. 1985

d. 1954

41 / 50

41. 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 manufacture of Medical device

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

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

42 / 50

42. Biological and Biotechnological products are included in schedule.

a. X

b. C and C1

c. B

d. A

43 / 50

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

a. Skin cosmetic preparation

b. Ointment formulation

c. Parenteral preparation

d. Ophthalmic preparation

44 / 50

44. 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

45 / 50

45. TGA is regulatory agency of………….

a. Zimbabwe

b. Australia

c. Denmark

d. India

46 / 50

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

a. FF

b. D

c. Q

d. A

47 / 50

47. Patent Act is established in

a. 1940

b. 1970

c. 1919

d. 1948

48 / 50

48. Aspirin sodium comes under

a. Schedule J

b. Schedule G

c. Schedule H

d. Schedule Y

49 / 50

49. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

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

d. Long time adverse effects aster marketing drug

50 / 50

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

a. S

b. O

c. R1

d. R

Your score is

The average score is 37%