Serious Adverse Events (SAEs): What it is and How to Handle 2015 is a webinar that covers topics such as:
- Department of Health and Human Services (DHHS) guidance
- ICH guidelines and Good Clinical Practice (GCP)
- Definitions
- Food and Drug Administration (FDA) guidance
- Examples
- Potential effects on consent and the protocol
- Links to useful resources
Serious Adverse Events (SAEs): What it is and How to Handle 2015 is intended for:
- Healthcare interested in exploring the field of Clinical Research
- Human Subjects Research
- New Principal Investigator Positions
- New Clinical Research Coordinator Positions (1-2 years)
- Regulatory Compliance
- Administration in charge of Clinical Research
