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

358

1 / 50

1. Example of Schedule G drug is

a. Enalapril

b. Barbital

c. Cefuroxime

d. Metformin

2 / 50

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

a. 20B

b. 20

c. 21

d. 21B

3 / 50

3. Biological and Biotechnological products are included in schedule.

a. A

b. B

c. C and C1

d. X

4 / 50

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

a. Four

b. Eight

c. Five

d. Six

5 / 50

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

a. Parenteral preparation

b. Ophthalmic preparation

c. Skin cosmetic preparation

d. Ointment formulation

6 / 50

6. 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 cool place

d. A Cold place

7 / 50

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

a. 150 square meters

b. 400 square meters

c. 250 square meters

d. 500 square meters

8 / 50

8. Patent Act is established in

a. 1970

b. 1919

c. 1940

d. 1948

9 / 50

9. In 1954 one of the following act is passed

a. The Medical Termination of pregnancy Act

b. Drug and magic Remedies Act

c. Narcotic and psychotropic substance Act

d. Poisonous Act.

10 / 50

10. Hatch Waxman Act is related to

a. Banned drugs

b. Over the counter drugs

c. Dangerous drugs Act

d. Spurious drugs Act

11 / 50

11. Drug and Magic Remedies Act is enacted in

a. 1954

b. 1948

c. 1985

d. 1919

12 / 50

12. Pack size of drug is covered under

a. Schedule P

b. Schedule P1

c. Schedule O

d. Schedule R

13 / 50

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

a. The officer in charge of drugs control organization

b. Chief Administrator medical officer of state

c. President of India

d. Government Analyst

14 / 50

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

a. 1955

b. 1985

c. 1950

d. 1940

15 / 50

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

a. Every 5 year

b. Every 2 year

c. Every 3 year

d. Every 6 year

16 / 50

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

a. Schedule Q

b. Schedule O

c. Schedule P

d. Schedule R

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. Spurious Drug

b. Adulterated Drug

c. Misbranded Drug

d. True Drug

18 / 50

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

a. 100 patients

b. 1-10 patients

c. 500 patients

d. 10-12 patients

19 / 50

19. Coca, opium and hemp come under:

a. Dangerous Drug Act

b. Spurious Drug Act

c. Insecticide Act

d. Poisons Act

20 / 50

20. Grant of licence to manufacture a drug requires.

a. Form 25

b. Form 24

c. Form 27

d. Form 26

21 / 50

21. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule L

c. Schedule K

d. Schedule J

22 / 50

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

a. Yellow

b. Blue

c. Red

d. White

23 / 50

23. TGA is regulatory agency of………….

a. Denmark

b. Zimbabwe

c. India

d. Australia

24 / 50

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

a. Ministry of Education

b. President, Pharmacy Council of India

c. Drug Controller

d. Central Government

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 H

b. Schedule I

c. Schedule G

d. Schedule J

26 / 50

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

a. Chief administrative medical officer of the state

b. All

c. Assistant drug controller

d. Chief pharmacist of government hospital

27 / 50

27. Purpose of Phase-3 trial is

a. Determine Possible therapeutic uses, Effective doses range

b. Long time adverse effects aster marketing drug

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

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

28 / 50

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

a. O

b. R1

c. R

d. S

29 / 50

29. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

30 / 50

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

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

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

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

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

31 / 50

31. Schedule J is related to

a. Pack sizes of drugs.

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

c. GMP

d. Curable disease

32 / 50

32. Schedule N states

a. Standard for cosmetics

b. Requirement of factory premises and hygienic condition to complied

c. List of minimum equipment for efficient running of pharmacy

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

33 / 50

33. 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

34 / 50

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

a. Q

b. A

c. D

d. FF

35 / 50

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

a. 3

b. 1

c. 2

d. 4

36 / 50

36. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. List of generic drugs

c. None of the above

d. List of incurable diseases

37 / 50

37. MHRA is regulatory agency of ……….....

a. Brazil

b. UK

c. Denmark

d. South Africa

38 / 50

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

a. Symbol X given in red

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

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

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

39 / 50

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

a. Nine

b. Five

c. Seven

d. Six

40 / 50

40. Dettol comes under

a. Schedule Q

b. Schedule N

c. Schedule O

d. Schedule P

41 / 50

41. Post marketing surveillance comes under clinical trial

a. Phase V

b. Phase III

c. Phase I

d. Phase II

42 / 50

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

a. Area for opening retail pharmacy

b. Area required to open wholesale drug store

c. List of minimum equipments for efficiently running pharmacy

d. List of maximum equipments for efficiently running pharmacy

43 / 50

43. MCC is regulatory agency of ……………

a. South Africa

b. UK

c. Brazil

d. Denmark

44 / 50

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

a. X

b. H

c. K

d. G

45 / 50

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

a. W

b. Y

c. X

d. V

46 / 50

46. Aspirin sodium comes under

a. Schedule G

b. Schedule H

c. Schedule Y

d. Schedule J

47 / 50

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

a. At temperature which not exceed 20°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 5°C

48 / 50

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

a. Misbranded drugs

b. Toilet preparations

c. Schedule ‘C’ ‘G’ drugs

d. Ayurvedic drugs

49 / 50

49. Schedule C is related to

a. List of Allopathic product

b. List of Ayurvedic product

c. List of Biological and Immunological product

d. List of Homeopathy product

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 O

b. Schedule F

c. Schedule Y

d. Schedule M

Your score is

The average score is 37%