Resource Library
Create, assemble, review, publish, and archive electronic submissions while ensuring compliance.
The EMC Documentum Regulatory Submissions for Life Sciences solution provides the infrastructure to create, assemble, review, publish, and archive electronic submissions while ensuring compliance. Gain Adobe Acrobat integration for PDF hyperlinking, manipulation, and auditing. Leverage encrypted file storage and digital shredding, and advanced PDF publishing capabilities such as merging, volumization, and stamping.
Key Benefits
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Streamlined review and approval process — Reduce the cost and complexity of regulatory submissions, and accelerate time to approval and time to market.
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Collaborative processes — Enable teams to plan, create, edit, and generate drafts, all managed in a central repository for review, approval, and publishing.
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Information accessibility — Enable information to be accessed quickly and reused for new submissions, and allow documents to be reviewed simultaneously by regulatory bodies.
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Infrastructure consolidation — Consolidate multiple archive technologies into a comprehensive, centrally managed electronic submission management workflow.
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Automated compliance — Automate compliance processes to reduce the risk of legal penalties while spending less on legal discovery, research, and prosecution.
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