Life Science

EMC DOCUMENTUM: DOCUMENT CONTROL FOR LIFE SCIENCES

Throughout the clinical trial and R&D process, Documentum document management can help ensure compliance, streamline processes, and boost productivity as the platform:

• Provides improved visibility into trial and regulatory submission documents

• Simplifies access and retrieval of documents

• Simplifies authoring, content management, and collaboration

• Ensures security and access control

• Minimizes compliance risk

Learn more below about how Documentum for Life Sciences can help you.

EMC DOCUMENTUM FOR LIFE SCIENCES – DOCUMENTUM ETMF

15-MINUTE GUIDE TO CLINICAL TRIAL DOCUMENT MANAGEMENT & ETMF

A well-designed eTMF can accelerate trial set up, deliver comprehensive document visibility during the trial, and streamline access to trial documents at the conclusion of the trial. EMC Documentum for Life Sciences delivers a unified, configurable document control platform for compliance with industry regulations. With the Documentum solution, you get auditing, reporting, and e-signature for compliances, lifecycle management and document control services, and industry-specific modeling capabilities all designed specifically for life sciences.

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