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

365

1 / 50

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

a. Blue

b. Red

c. White

d. Yellow

2 / 50

2. Biological and Biotechnological products are included in schedule.

a. X

b. B

c. C and C1

d. A

3 / 50

3. 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. X

d. H

4 / 50

4. In 1954 one of the following act is passed

a. Poisonous Act.

b. The Medical Termination of pregnancy Act

c. Narcotic and psychotropic substance Act

d. Drug and magic Remedies Act

5 / 50

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

a. Schedule Q

b. Schedule R

c. Schedule O

d. Schedule P

6 / 50

6. Aspirin sodium comes under

a. Schedule Y

b. Schedule G

c. Schedule H

d. Schedule J

7 / 50

7. 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. X

d. V

8 / 50

8. 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. Misbranded Drug

c. Adulterated Drug

d. Spurious Drug

9 / 50

9. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

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

c. Long time adverse effects aster marketing drug

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

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 O

b. Schedule F

c. Schedule Y

d. Schedule M

11 / 50

11. MHRA is regulatory agency of ……….....

a. UK

b. South Africa

c. Denmark

d. Brazil

12 / 50

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

a. List of prescription drugs

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

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

d. Requirements of factory premises

13 / 50

13. Example of Schedule G drug is

a. Enalapril

b. Metformin

c. Cefuroxime

d. Barbital

14 / 50

14. 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

15 / 50

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

a. Six

b. Eight

c. Four

d. Five

16 / 50

16. Kala jadu or Kavach comes under

a. Schedule K

b. Schedule J

c. Schedule L

d. Schedule P

17 / 50

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

a. Q

b. A

c. D

d. FF

18 / 50

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

a. R

b. S

c. O

d. R1

19 / 50

19. Post marketing surveillance comes under clinical trial

a. Phase I

b. Phase III

c. Phase V

d. Phase II

20 / 50

20. TGA is regulatory agency of………….

a. Denmark

b. Australia

c. Zimbabwe

d. India

21 / 50

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

a. 500 square meters

b. 150 square meters

c. 400 square meters

d. 250 square meters

22 / 50

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

a. Area required to open wholesale drug store

b. List of minimum equipments for efficiently running pharmacy

c. List of maximum equipments for efficiently running pharmacy

d. Area for opening retail pharmacy

23 / 50

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

a. Toilet preparations

b. Schedule ‘C’ ‘G’ drugs

c. Misbranded drugs

d. Ayurvedic drugs

24 / 50

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

a. Seven

b. Nine

c. Five

d. Six

25 / 50

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

a. 500 patients

b. 10-12 patients

c. 100 patients

d. 1-10 patients

26 / 50

26. Schedule N states

a. Requirement of factory premises and hygienic condition to complied

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

c. Standard for cosmetics

d. List of minimum equipment for efficient running of pharmacy

27 / 50

27. Patent Act is established in

a. 1940

b. 1919

c. 1970

d. 1948

28 / 50

28. MCC is regulatory agency of ……………

a. UK

b. Brazil

c. South Africa

d. Denmark

29 / 50

29. 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

30 / 50

30. 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

31 / 50

31. Drug and Magic Remedies Act is enacted in

a. 1985

b. 1919

c. 1948

d. 1954

32 / 50

32. Injection syringe and needles are covered under

a. Schedule A

b. Schedule B

c. Schedule P

d. Schedule Q

33 / 50

33. Dettol comes under

a. Schedule O

b. Schedule P

c. Schedule Q

d. Schedule N

34 / 50

34. Hatch Waxman Act is related to

a. Spurious drugs Act

b. Dangerous drugs Act

c. Banned drugs

d. Over the counter drugs

35 / 50

35. 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

36 / 50

36. Pack size of drug is covered under

a. Schedule P

b. Schedule O

c. Schedule P1

d. Schedule R

37 / 50

37. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Insecticide Act

c. Spurious Drug Act

d. Poisons Act

38 / 50

38. Grant of licence to manufacture a drug requires.

a. Form 27

b. Form 24

c. Form 25

d. Form 26

39 / 50

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

a. 1

b. 4

c. 2

d. 3

40 / 50

40. 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 H displayed on right top corner of the label.

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

d. Symbol X given in red

41 / 50

41. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Homeopathy product

d. List of Biological and Immunological product

42 / 50

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

a. Parenteral preparation

b. Skin cosmetic preparation

c. Ophthalmic preparation

d. Ointment formulation

43 / 50

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

a. At temperature which not exceed 20°C

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. In cold place

44 / 50

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

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

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 manufacturer of Ayurveda, Sidhha and Unani drugs

45 / 50

45. Schedule J is related to

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

b. GMP

c. Pack sizes of drugs.

d. Curable disease

46 / 50

46. Schedule X of Drugs and Cosmetics Act comprises

a. List of generic drugs

b. List of incurable diseases

c. None of the above

d. Guidelines for clinical Trials

47 / 50

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

a. Central Government

b. Drug Controller

c. President, Pharmacy Council of India

d. Ministry of Education

48 / 50

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

a. Chief Administrator medical officer of state

b. The officer in charge of drugs control organization

c. President of India

d. Government Analyst

49 / 50

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

a. 1940

b. 1985

c. 1955

d. 1950

50 / 50

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

a. Every 6 year

b. Every 2 year

c. Every 3 year

d. Every 5 year

Your score is

The average score is 38%