- Discover ITHS
- About ITHS
- About Translational Research
- Leadership
- ITHS Cores
- Administration
- Biomedical Informatics
- Center for Biomedical Statistics
- Center for Scientific Review
- Clinical Research Center Network
- Community Outreach and Research Translation
- Evaluation Research
- Preclinical Research Development Network
- Regulatory Support and Bioethics
- Research Education, Training, & Career Dev.
- Strategic Development
- Translational Technologies and Resources
- WWAMI Translational Research Consortium
- Regional Partnerships
- Accomplishments
- Request a CONSULT
- Find a RESOURCE
- Get FUNDING
- Find TRAINING
- Find PEOPLE
- Get INVOLVED
Adverse Events in Clinical Research – the what, when and how of reporting
Date and time:
Wed, 09/10/2008 - 12:00pm - 1:00pm
Location:
Turner Auditorium, D-209, UW Presenter:
Ann J. Melvin, MD, MPH
Director, ITHS Regulatory Support and Bioethics Core
Objectives:
- Clarifying AE definitions
- Understanding AE grading and attribution
- Meeting responsibilities for AE reporting
Presented materials:
