Life sciences organizations face more pressure than ever to run efficient, uninterrupted manufacturing production at the lowest possible cost, while meeting stringent safety, quality and regulatory standards to ensure patient safety. Production delays can cost millions of dollars per day while consent decree fines for violations of Good Manufacturing Processes (GMP) standards can be exorbitant.
The OpenText Quality and Manufacturing solution, part of the OpenText for Life Sciences solution suite, enables life sciences organizations to control quality and manufacturing documents, automate workflows across the extended enterprise, and ensure compliance with GMP standards. The solution enables auditing, reporting, and e-signature support for compliance, lifecycle management, and document control services, and industry-specific modeling capabilities.
For the extended enterprise operating across geographies and with external partners, the solution enhances the productivity and virtualization of your global supply chain with streamlined workflows, bullet-proof security models and collaboration capabilities.
The foundation of the solution includes the Documentum® Enterprise Content Management platform, Documentum® D2 for configuration and intuitive user interfaces, implementation and migration services.