EMC Documentum Research and Development Solution
- Pharmaceutical companies
- Contract development companies
- Regulatory operations
- Ensure all documents are submission-ready
- Streamline submission document review and approval
- Improve author productivity for submissions
Improve Document Accuracy
Streamline Review Process
Increase Author Productivity
Minimize Compliance Risk
Driven by expiring patents and shrinking drug-development pipelines as new therapies become fewer and more intricate, most life sciences companies need to continually streamline their regulatory submissions process to deliver new products to market faster. They need a robust content repository to manage what can be millions of documents while maintaining compliance with regulatory requirements.
Companies also need the ability to effectively plan, track, maintain, and assemble essential submission-related documentation. This constantly growing collection of controlled documentation is the primary knowledge asset and is the key to the future success of the organization.
The EMC Documentum Research and Development solution, part of the EMC Documentum for Life Sciences solution suite, enables organizations to manage the creation, review, and approval of regulatory submission documentation. The solution provides predefined taxonomies and business process rules to reduce deployment time and ensure adherence to industry standards while collaborative authoring capabilities improve productivity and streamline review and approval processes.
With the Research and Development solution, users can quickly search and identify submission-ready content across multiple EMC Documentum for Life Sciences solutions such as the EMC Documentum Electronic Trial Master File (eTMF) and EMC Documentum Quality and Manufacturing (Q&M) solutions for more efficient regulatory submission assembly. The foundation of this solution includes the EMC Documentum enterprise content management platform and EMC Documentum D2 for configuration and intuitive user interfaces, implementation, and migration services.
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Manage sensitive information wherever it resides to ensure document security.
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Automate content-intensive business processes to increase operational efficiency, make better decisions, and reduce risk.
Preserve the value of enterprise data and content to comply with retention requirements in an easily accessible, unified archive.
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EMC Documentum Electronic Trial Master File Solution
Improve productivity and accelerate clinical trial documentation.
EMC Documentum Quality and Manufacturing Solution
Gain control of documentation, automate workflows across the enterprise and ensure GMP compliance with EMC Documentum Quality and Manufacturing
EMC Managed Services OnDemand
Deploy content management solutions powered by private cloud technology to achieve greater agility, lower risk, and predictable cost management.
- A 15-Minute Guide to Clinical Trial Document Management and the eTMF
- 15-Minute Guide to Efficient and Compliant Management of GMP Controlled Documents
- 15-Minute Guide to Protecting and Controlling Content Wherever it Resides
- Assuring Life Sciences Compliance in the Private Cloud
- EMC Consulting Regulated Information Management for Life Sciences
News & Blogs
Jan 08, 2013EMC Helps Leading Vaccine Manufacturer Boost IT Efficiency; Reduces TCO 20% with Life Sciences Solution
May 22, 2012EMC Delivers Information Management Software and Solutions to Accelerate Customers’ Journey to the Cloud and Transform Business Processes
May 22, 2012EMC Delivers Documentum Solution Suite for Life Sciences