As of January 1, 2008, the U.S. FDA will only accept electronic submissions in eCTD format and European agencies are soon to follow. Are you prepared to meet these requirements?

For mid-sized life sciences companies and large pharmaceuticals looking to jumpstart enterprise deployments, Compliance-in-a-Box Submission Edition can help. Developed by EMC, ISI, and Impact Systems, this affordable and cost-effective solution includes EMC Documentum Compliance Manager, preconfigured for regulatory submissions applications, integrated with ISI eCTDXpress, for submitting electronic content to worldwide regulatory agencies.

Register to view this recorded webcast to see how you can manage controlled content seamlessly—from authoring to submission

During this recorded webcast, you’ll see a demonstration of Compliance-in-a-Box Submission Edition and learn how to:

• Automate the entire document lifecycle—from authoring and document publishing to submission creation and archiving of the complete submission
• Significantly reduce implementation time with Documentum Compliance Manager preconfigured for regulatory submissions
• Integrate controlled content management, submissions, and publishing to optimize the submission process and greatly reduce costs
• Preserve audit trail information from document creation to final submission, ensuring adherence to regulatory requirements