What are Serious Adverse Events & How do I Handle SAEs? 2014
19 Nov 2014
Webinar
Description
Topics
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
Who should Attend
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
Past Events
What are Serious Adverse Events & How do I Handle SAEs? 2014 - 19 Nov 2014, Webinar (32528)
Important
Please, check "What are Serious Adverse Events & How do I Handle SAEs?" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical laboratories, Pharma
