The Common Serious Adverse Events (SAE) Fields Initiative intends to conduct a feasibility assessment, develop best practices relating to identifying the most critical SAE fields, and work with an industry standard setting organization to promulgate standards in this area, all with the intent of increasing the quality of what is reported and creating efficiencies for sites, CROs and regulators.
- Supply Health Authorities and an industry standard-setting organization with a proposed common core list of SAE fields to help create an SAE data collection industry standard
- Supports the complete clinical presentation of an SAE
- Allows for independent clinical assessments
- Positively impacts patient safety, investigators, health authorities and sponsors
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