The safety and pharmacovigilance landscape is changing rapidly, and the new global standards for regulatory reporting – E2B(R3), eVAERS, eMDR, and IDMP – represent some of the most significant changes that the industry has seen in over a decade. Not surprisingly, implementing them requires planning and preparation from both safety and IT organizations.
 
Oracle Health Sciences’ safety strategists, product managers, and solution experts have looked at the impact that these changes will have, as well as how best to prepare for them, and their findings have been presented in a 60-minute webcast covering the following topics:

• Overview of the known compliance timelines for the new standards
• Highlights of the impact on life sciences organizations
• Strategic preparation for regulatory changes th
• Demo of E2B(R3) functionality in Oracle Argus 8.0

Click here to play back the webcast recording, and here to download a summary brief to help you prepare for these changes.