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. Biological and Biotechnological products are included in schedule.

a. C and C1

b. X

c. B

d. A

2 / 50

2. Grant of licence to manufacture a drug requires.

a. Form 26

b. Form 24

c. Form 25

d. Form 27

3 / 50

3. 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

4 / 50

4. 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

5 / 50

5. Coca, opium and hemp come under:

a. Insecticide Act

b. Dangerous Drug Act

c. Poisons Act

d. Spurious Drug Act

6 / 50

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

a. 21

b. 20

c. 20B

d. 21B

7 / 50

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

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

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

c. Requirements of factory premises

d. List of prescription drugs

8 / 50

8. 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.

9 / 50

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

a. Chief Administrator medical officer of state

b. President of India

c. The officer in charge of drugs control organization

d. Government Analyst

10 / 50

10. Injection syringe and needles are covered under

a. Schedule P

b. Schedule Q

c. Schedule A

d. Schedule B

11 / 50

11. 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

12 / 50

12. 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 M

d. Schedule F

13 / 50

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

a. Ayurvedic drugs

b. Misbranded drugs

c. Schedule ‘C’ ‘G’ drugs

d. Toilet preparations

14 / 50

14. Patent Act is established in

a. 1940

b. 1970

c. 1948

d. 1919

15 / 50

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

a. R1

b. O

c. R

d. S

16 / 50

16. Hatch Waxman Act is related to

a. Dangerous drugs Act

b. Banned drugs

c. Spurious drugs Act

d. Over the counter drugs

17 / 50

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

a. G

b. K

c. H

d. X

18 / 50

18. 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 20°C

c. In cold place

d. At temperature which not exceed 5°C

19 / 50

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

d. Long time adverse effects aster marketing drug

20 / 50

20. MHRA is regulatory agency of ……….....

a. UK

b. Brazil

c. Denmark

d. South Africa

21 / 50

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

a. White

b. Yellow

c. Red

d. Blue

22 / 50

22. Schedule N states

a. List of minimum equipment for efficient running of pharmacy

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

c. Standard for cosmetics

d. Requirement of factory premises and hygienic condition to complied

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. Y

b. V

c. X

d. W

24 / 50

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

a. 4

b. 3

c. 2

d. 1

25 / 50

25. Dettol comes under

a. Schedule Q

b. Schedule O

c. Schedule N

d. Schedule P

26 / 50

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

a. Six

b. Five

c. Four

d. Eight

27 / 50

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

a. Schedule R

b. Schedule Q

c. Schedule P

d. Schedule O

28 / 50

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

a. Seven

b. Six

c. Five

d. Nine

29 / 50

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

a. 1950

b. 1985

c. 1940

d. 1955

30 / 50

30. TGA is regulatory agency of………….

a. India

b. Denmark

c. Zimbabwe

d. Australia

31 / 50

31. 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

32 / 50

32. MCC is regulatory agency of ……………

a. UK

b. South Africa

c. Denmark

d. Brazil

33 / 50

33. Schedule J is related to

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

b. Pack sizes of drugs.

c. Curable disease

d. GMP

34 / 50

34. Post marketing surveillance comes under clinical trial

a. Phase III

b. Phase I

c. Phase V

d. Phase II

35 / 50

35. Kala jadu or Kavach comes under

a. Schedule P

b. Schedule K

c. Schedule J

d. Schedule L

36 / 50

36. Schedule X of Drugs and Cosmetics Act comprises

a. Guidelines for clinical Trials

b. None of the above

c. List of incurable diseases

d. List of generic drugs

37 / 50

37. Schedule C is related to

a. List of Allopathic product

b. List of Biological and Immunological product

c. List of Homeopathy product

d. List of Ayurvedic product

38 / 50

38. 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. True Drug

c. Misbranded Drug

d. Spurious Drug

39 / 50

39. 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 maximum equipments for efficiently running pharmacy

d. List of minimum equipments for efficiently running pharmacy

40 / 50

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

a. Drug Controller

b. President, Pharmacy Council of India

c. Central Government

d. Ministry of Education

41 / 50

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

a. Ointment formulation

b. Parenteral preparation

c. Skin cosmetic preparation

d. Ophthalmic preparation

42 / 50

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

a. Every 5 year

b. Every 2 year

c. Every 3 year

d. Every 6 year

43 / 50

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

a. A Cold place

b. Temperature not exceeding 5°C

c. A cool place

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

44 / 50

44. Pack size of drug is covered under

a. Schedule P1

b. Schedule O

c. Schedule P

d. Schedule R

45 / 50

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

a. A

b. Q

c. D

d. FF

46 / 50

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

a. All

b. Chief pharmacist of government hospital

c. Assistant drug controller

d. Chief administrative medical officer of the state

47 / 50

47. 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

48 / 50

48. Aspirin sodium comes under

a. Schedule H

b. Schedule Y

c. Schedule G

d. Schedule J

49 / 50

49. Drug and Magic Remedies Act is enacted in

a. 1948

b. 1919

c. 1954

d. 1985

50 / 50

50. Example of Schedule G drug is

a. Cefuroxime

b. Barbital

c. Enalapril

d. Metformin

Your score is

The average score is 37%