Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test Noteskarts

Pharmacy Law & Ethics & Pharmaceutical Jurisprudence | Pharmacy Law & Ethics DPEE Test

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

169

1 / 50

1. Aspirin sodium comes under

a. Schedule G

b. Schedule Y

c. Schedule J

d. Schedule H

2 / 50

2. Injection syringe and needles are covered under

a. Schedule A

b. Schedule P

c. Schedule B

d. Schedule Q

3 / 50

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

a. In cold place

b. At temperature which not exceed 20°C

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

d. At temperature which not exceed 5°C

4 / 50

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

a. 1940

b. 1955

c. 1950

d. 1985

5 / 50

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

a. S

b. R1

c. R

d. O

6 / 50

6. Schedule C is related to

a. List of Biological and Immunological product

b. List of Homeopathy product

c. List of Ayurvedic product

d. List of Allopathic product

7 / 50

7. 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

8 / 50

8. 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. 21B

d. 20

9 / 50

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

a. Area required to open wholesale drug store

b. Area for opening retail pharmacy

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

10 / 50

10. MCC is regulatory agency of ……………

a. Denmark

b. Brazil

c. South Africa

d. UK

11 / 50

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

a. 1

b. 4

c. 3

d. 2

12 / 50

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

a. White

b. Red

c. Yellow

d. Blue

13 / 50

13. Pack size of drug is covered under

a. Schedule P1

b. Schedule R

c. Schedule P

d. Schedule O

14 / 50

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

a. 500 patients

b. 100 patients

c. 1-10 patients

d. 10-12 patients

15 / 50

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

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

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

c. List of prescription drugs

d. Requirements of factory premises

16 / 50

16. Kala jadu or Kavach comes under

a. Schedule L

b. Schedule J

c. Schedule K

d. Schedule P

17 / 50

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

a. A Cold place

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

c. A cool place

d. Temperature not exceeding 5°C

18 / 50

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

a. Ointment formulation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Parenteral preparation

19 / 50

19. Coca, opium and hemp come under:

a. Spurious Drug Act

b. Poisons Act

c. Insecticide Act

d. Dangerous Drug Act

20 / 50

20. 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

21 / 50

21. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase V

c. Phase II

d. Phase I

22 / 50

22. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Over the counter drugs

d. Spurious drugs Act

23 / 50

23. Purpose of Phase-3 trial is

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

b. Long time adverse effects aster marketing drug

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

d. Determine Possible therapeutic uses, Effective doses range

24 / 50

24. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Metformin

d. Cefuroxime

25 / 50

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

a. Chief administrative medical officer of the state

b. Assistant drug controller

c. Chief pharmacist of government hospital

d. All

26 / 50

26. Dettol comes under

a. Schedule P

b. Schedule Q

c. Schedule N

d. Schedule O

27 / 50

27. 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 Ayurveda, Sidhha and Unani drugs

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

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

28 / 50

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

a. Toilet preparations

b. Ayurvedic drugs

c. Misbranded drugs

d. Schedule ‘C’ ‘G’ drugs

29 / 50

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

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

b. Symbol N 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

30 / 50

30. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 26

c. Form 27

d. Form 25

31 / 50

31. 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 J

c. Schedule H

d. Schedule G

32 / 50

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

a. X

b. G

c. K

d. H

33 / 50

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

a. Every 6 year

b. Every 2 year

c. Every 3 year

d. Every 5 year

34 / 50

34. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. None of the above

c. Guidelines for clinical Trials

d. List of incurable diseases

35 / 50

35. 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. Spurious Drug

c. True Drug

d. Misbranded Drug

36 / 50

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

a. The officer in charge of drugs control organization

b. President of India

c. Chief Administrator medical officer of state

d. Government Analyst

37 / 50

37. Schedule N states

a. Standard for cosmetics

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

c. List of minimum equipment for efficient running of pharmacy

d. Requirement of factory premises and hygienic condition to complied

38 / 50

38. 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 M

d. Schedule O

39 / 50

39. TGA is regulatory agency of………….

a. Australia

b. India

c. Denmark

d. Zimbabwe

40 / 50

40. MHRA is regulatory agency of ……….....

a. South Africa

b. Brazil

c. Denmark

d. UK

41 / 50

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

a. Eight

b. Six

c. Five

d. Four

42 / 50

42. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1954

c. 1919

d. 1985

43 / 50

43. Schedule J is related to

a. Pack sizes of drugs.

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

c. Curable disease

d. GMP

44 / 50

44. Patent Act is established in

a. 1940

b. 1919

c. 1948

d. 1970

45 / 50

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

a. Schedule Q

b. Schedule P

c. Schedule R

d. Schedule O

46 / 50

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

a. FF

b. D

c. Q

d. A

47 / 50

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

a. Ministry of Education

b. Drug Controller

c. President, Pharmacy Council of India

d. Central Government

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. Y

b. W

c. V

d. X

49 / 50

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

a. Nine

b. Seven

c. Five

d. Six

50 / 50

50. Biological and Biotechnological products are included in schedule.

a. C and C1

b. A

c. X

d. B

Your score is

The average score is 31%