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Scanned documents have always been a part of regulatory submissions. Although most companies strive to replace scanned documents with authored documents to the greatest extent possible, eCTDs into the future will continue to include scanned documents – but the bar has been raised as far as the required quality.
Learn about considerations and best practices for scanning, indexing and QC’ing your scanned documents to ensure a high quality eCTD submission.
When & Where
Webcast Event
Conference Call,
19103
Wednesday, July 23, 2008 from 11:00 AM to 12:00 PM (ET)
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Hosted By
GlobalSubmit Product Team
GlobalSubmit is a products and services company that provides transparency in regulated healthcare products. The U.S. Food & Drug Administration and leading life sciences companies use our flagship applications, REVIEW™ and VALIDATE™, to review and validate electronic submissions. GlobalSubmit leads international efforts, comprising industry and government agencies, to standardize product and study information. The company is headquartered in Philadelphia, Pennsylvania.
