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1
Intro
2
DRAFTING THE PROTOCOL
3
STUDY AGENT OVERVIEW
4
STUDY DESIGN
5
CASE QUESTIONS: STUDY POPULATION
6
CASE EXAMPLE: EXCLUSION CRITERIA
7
STUDY SCHEDULE AND PROCEDURES
8
CASE QUESTIONS: SCHEDULE OF PROCEDURES
9
CASE EXAMPLE: SCHEDULE OF PROCEDURES
10
PART 2: THE COMPLEXITY OF PROTOCOL LOGISTICS
11
SAFETY OVERSIGHT AND DATA CAPTURE
12
CASE QUESTIONS: LOGISTICS
Description:
Explore protocol development and implementation in clinical and translational research through a 48-minute lecture from the NIH Clinical Center's summer course. Delve into drafting protocols, study agent overviews, and study design. Examine case studies on study populations, exclusion criteria, and scheduling procedures. Investigate the complexities of protocol logistics, safety oversight, and data capture. Gain insights into unique NIH resources, connect with researchers and program administrators, and discover potential NIH career opportunities. For further information about this comprehensive learning experience, contact the course coordinator at [email protected].

Protocol Development and Implementation - Lecture 6

NIH Clinical Center
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