2013년 10월 27일 일요일

임상실험 (Clinical Trials) (영문)

임상실험 (Clinical Trials) (영문)
임상실험 (Clinical Trials) (영문).ppt


목차
Introduction of Clinical Trials
Protocols and IRB
PhaseⅠ
PhaseⅡ
PhaseⅢ
PhaseⅣ


본문
Clinical test

Clinicaltrialislimitedtohuman,thereforeitisthepreconditionthatensuringethicality withscientificvalidityofstudy.

Necessity of Clinical test
- Developing a new drug for Korean inherited trait
- Offering the earliest opportunity to patients
- Strengthening the capability of researchers
- Clinical trial has high added value

It is a plan that recorded specific details
How clinical trials should be performed

Including all aspects of the research study
participant inclusion / exclusion criteria
test schedules and procedures
medications and their dosages
methods used to analyze the data collected

- By protocols, experiment could get validity


본문내용

PhaseⅢ
PhaseⅣ

PhaseⅣ
Clinical test
Clinical trial is limited to human, therefore it is the precondition that ensuring ethicality with scientific validity of study.
research side effect to prove safety
and validation of medicine

Necessity of Clinical test
- Developing a new drug for Korean inherited trait
- Offering the earliest opportunity to patients
- Strengthening the capability of researche
 

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