임상실험(Clinical Trials)(영문)
- 등록일 / 수정일
- 페이지 / 형식
- 자료평가
- 구매가격
- 2012.11.12 / 2019.12.24
- 19페이지 / ppt (파워포인트 2003)
- 평가한 분이 없습니다. (구매금액의 3%지급)
- 1,500원
최대 20페이지까지 미리보기 서비스를 제공합니다.
자료평가하면 구매금액의 3%지급!
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추천 연관자료
- 목차
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Introduction of Clinical Trials
Protocols and IRB
PhaseⅠ
PhaseⅡ
PhaseⅢ
PhaseⅣ
- 본문내용
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Clinical test
Clinical trial is limited to human, therefore it is the precondition that ensuring ethicality with scientific validity of study.
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
자료평가
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아직 평가한 내용이 없습니다.