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

366

1 / 50

1. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule P

c. Schedule L

d. Schedule J

2 / 50

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

a. G

b. H

c. K

d. X

3 / 50

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

a. Q

b. FF

c. D

d. A

4 / 50

4. Example of Schedule G drug is

a. Metformin

b. Barbital

c. Cefuroxime

d. Enalapril

5 / 50

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

a. 21

b. 21B

c. 20

d. 20B

6 / 50

6. Grant of licence to manufacture a drug requires.

a. Form 24

b. Form 25

c. Form 27

d. Form 26

7 / 50

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

a. 1985

b. 1955

c. 1940

d. 1950

8 / 50

8. Biological and Biotechnological products are included in schedule.

a. A

b. C and C1

c. X

d. B

9 / 50

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

a. Government Analyst

b. President of India

c. The officer in charge of drugs control organization

d. Chief Administrator medical officer of state

10 / 50

10. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

b. List of minimum equipment for efficient running of pharmacy

c. Standard for cosmetics

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

11 / 50

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

a. Schedule P

b. Schedule O

c. Schedule R

d. Schedule Q

12 / 50

12. 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 5°C

c. At temperature which not exceed 20°C

d. In cold place

13 / 50

13. 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. All

d. Chief pharmacist of government hospital

14 / 50

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

a. Every 2 year

b. Every 6 year

c. Every 5 year

d. Every 3 year

15 / 50

15. MHRA is regulatory agency of ……….....

a. Brazil

b. Denmark

c. UK

d. South Africa

16 / 50

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

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

b. Requirements of factory premises

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

d. List of prescription drugs

17 / 50

17. 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. Adulterated Drug

d. Misbranded Drug

18 / 50

18. 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 O

d. Schedule M

19 / 50

19. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Spurious Drug Act

d. Poisons Act

20 / 50

20. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase V

c. Phase III

d. Phase II

21 / 50

21. MCC is regulatory agency of ……………

a. Denmark

b. UK

c. South Africa

d. Brazil

22 / 50

22. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

23 / 50

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

a. R

b. S

c. O

d. R1

24 / 50

24. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

25 / 50

25. 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

26 / 50

26. 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

27 / 50

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

a. Six

b. Nine

c. Seven

d. Five

28 / 50

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

a. Red

b. Blue

c. Yellow

d. White

29 / 50

29. 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 Allopathy drugs

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

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

30 / 50

30. 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

31 / 50

31. Schedule X of Drugs and Cosmetics Act comprises

a. List of incurable diseases

b. List of generic drugs

c. Guidelines for clinical Trials

d. None of the above

32 / 50

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

a. Toilet preparations

b. Schedule ‘C’ ‘G’ drugs

c. Ayurvedic drugs

d. Misbranded drugs

33 / 50

33. Purpose of Phase-3 trial is

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

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

c. Long time adverse effects aster marketing drug

d. Determine Possible therapeutic uses, Effective doses range

34 / 50

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

a. Ophthalmic preparation

b. Skin cosmetic preparation

c. Parenteral preparation

d. Ointment formulation

35 / 50

35. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Over the counter drugs

d. Banned drugs

36 / 50

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

a. 1

b. 4

c. 2

d. 3

37 / 50

37. 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

38 / 50

38. Dettol comes under

a. Schedule N

b. Schedule P

c. Schedule Q

d. Schedule O

39 / 50

39. Aspirin sodium comes under

a. Schedule Y

b. Schedule H

c. Schedule J

d. Schedule G

40 / 50

40. Pack size of drug is covered under

a. Schedule O

b. Schedule P

c. Schedule P1

d. Schedule R

41 / 50

41. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. Zimbabwe

d. India

42 / 50

42. 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

43 / 50

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

a. List of minimum equipments for efficiently running pharmacy

b. List of maximum equipments for efficiently running pharmacy

c. Area for opening retail pharmacy

d. Area required to open wholesale drug store

44 / 50

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

a. 10-12 patients

b. 100 patients

c. 500 patients

d. 1-10 patients

45 / 50

45. 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

46 / 50

46. Patent Act is established in

a. 1970

b. 1948

c. 1919

d. 1940

47 / 50

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

c. Symbol X given in red

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

48 / 50

48. Schedule C is related to

a. List of Ayurvedic product

b. List of Allopathic product

c. List of Homeopathy product

d. List of Biological and Immunological product

49 / 50

49. In 1954 one of the following act is passed

a. Drug and magic Remedies Act

b. Poisonous Act.

c. Narcotic and psychotropic substance Act

d. The Medical Termination of pregnancy Act

50 / 50

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

a. Six

b. Five

c. Four

d. Eight

Your score is

The average score is 38%