The What are Serious Adverse Events & How do I Handle SAEs? 2014 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
The What are Serious Adverse Events & How do I Handle SAEs? 2014 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
