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

169

1 / 50

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

a. Schedule ‘C’ ‘G’ drugs

b. Toilet preparations

c. Ayurvedic drugs

d. Misbranded drugs

2 / 50

2. Schedule J is related to

a. Curable disease

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

c. GMP

d. Pack sizes of drugs.

3 / 50

3. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Denmark

d. Brazil

4 / 50

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

a. Schedule R

b. Schedule Q

c. Schedule O

d. Schedule P

5 / 50

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

a. 1950

b. 1985

c. 1955

d. 1940

6 / 50

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

a. Ministry of Education

b. Central Government

c. Drug Controller

d. President, Pharmacy Council of India

7 / 50

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

a. President of India

b. The officer in charge of drugs control organization

c. Chief Administrator medical officer of state

d. Government Analyst

8 / 50

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

a. Assistant drug controller

b. Chief pharmacist of government hospital

c. All

d. Chief administrative medical officer of the state

9 / 50

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

a. X

b. K

c. H

d. G

10 / 50

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

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

b. Symbol X given in red

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

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

11 / 50

11. As per D and C act schedule T stated about

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

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

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

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

12 / 50

12. Pack size of drug is covered under

a. Schedule R

b. Schedule P

c. Schedule O

d. Schedule P1

13 / 50

13. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. B

d. X

14 / 50

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

a. Four

b. Eight

c. Five

d. Six

15 / 50

15. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. Guidelines for clinical Trials

c. List of incurable diseases

d. None of the above

16 / 50

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

a. 250 square meters

b. 400 square meters

c. 150 square meters

d. 500 square meters

17 / 50

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

a. Yellow

b. White

c. Red

d. Blue

18 / 50

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

a. Every 5 year

b. Every 3 year

c. Every 2 year

d. Every 6 year

19 / 50

19. Hatch Waxman Act is related to

a. Over the counter drugs

b. Dangerous drugs Act

c. Spurious drugs Act

d. Banned drugs

20 / 50

20. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase II

c. Phase III

d. Phase V

21 / 50

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

a. 10-12 patients

b. 500 patients

c. 1-10 patients

d. 100 patients

22 / 50

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

d. Requirements of factory premises

23 / 50

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

a. V

b. W

c. X

d. Y

24 / 50

24. Coca, opium and hemp come under:

a. Poisons Act

b. Spurious Drug Act

c. Insecticide Act

d. Dangerous Drug Act

25 / 50

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

a. A cool place

b. A Cold place

c. Temperature not exceeding 5°C

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

26 / 50

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

a. Five

b. Six

c. Nine

d. Seven

27 / 50

27. Schedule N states

a. Standard for cosmetics

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

c. Requirement of factory premises and hygienic condition to complied

d. List of minimum equipment for efficient running of pharmacy

28 / 50

28. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

29 / 50

29. Dettol comes under

a. Schedule P

b. Schedule N

c. Schedule Q

d. Schedule O

30 / 50

30. Kala jadu or Kavach comes under

a. Schedule J

b. Schedule L

c. Schedule K

d. Schedule P

31 / 50

31. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule J

d. Schedule G

32 / 50

32. Patent Act is established in

a. 1970

b. 1940

c. 1919

d. 1948

33 / 50

33. Example of Schedule G drug is

a. Metformin

b. Cefuroxime

c. Barbital

d. Enalapril

34 / 50

34. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

35 / 50

35. List of drugs which should be used by patient under medical supervision is covered under………..as per D & C Act.

a. Schedule G

b. Schedule I

c. Schedule J

d. Schedule H

36 / 50

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

a. 4

b. 3

c. 1

d. 2

37 / 50

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

a. Ophthalmic preparation

b. Parenteral preparation

c. Ointment formulation

d. Skin cosmetic preparation

38 / 50

38. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1985

d. 1919

39 / 50

39. 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. Area for opening retail pharmacy

d. List of maximum equipments for efficiently running pharmacy

40 / 50

40. Purpose of Phase-3 trial is

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

b. Determine Possible therapeutic uses, Effective doses range

c. Long time adverse effects aster marketing drug

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

41 / 50

41. TGA is regulatory agency of………….

a. India

b. Zimbabwe

c. Denmark

d. Australia

42 / 50

42. Schedule C is related to

a. List of Homeopathy product

b. List of Allopathic product

c. List of Ayurvedic product

d. List of Biological and Immunological product

43 / 50

43. In 1954 one of the following act is passed

a. Narcotic and psychotropic substance Act

b. The Medical Termination of pregnancy Act

c. Poisonous Act.

d. Drug and magic Remedies Act

44 / 50

44. MCC is regulatory agency of ……………

a. Brazil

b. Denmark

c. South Africa

d. UK

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. Spurious Drug

b. True Drug

c. Adulterated Drug

d. Misbranded Drug

46 / 50

46. 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

47 / 50

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

a. Q

b. FF

c. A

d. D

48 / 50

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

a. At temperature which not exceed 5°C

b. In cold place

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

d. At temperature which not exceed 20°C

49 / 50

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

a. R

b. R1

c. S

d. O

50 / 50

50. 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 O

c. Schedule F

d. Schedule M

Your score is

The average score is 31%