With upcoming changes, including the implementation of E2B(R3) and IDMP standards, the current state of safety reporting in clinical trials can be confusing. Your existing safety system may not be flexible enough to accommodate these changing regulations, which are still moving targets in the details needed for a comprehensive solution with the right level of processes, company-to-company integrations and finalized regional rules.
Your end-to-end safety solution needs to encompass the required service, product and technology components in order to stand up to the challenges. Many vendors claim to have such a solution, but where do you start, and what is the best solution for your situation?
Download our white paper to learn more about:
- The current state of safety reporting and why it has been confusing
- Available solutions and the challenges they still pose
- Qualities of an ideal safety partner that blends services, technology and people to your capabilities and needs