EMC Documentum for Life Sciences

Documentum for Life Sciences on the basis of the EMC Documentum system represents the unified configured platform for management of documents according to industry requirements.

Platform

At the heart of the solution — the Documentum Enterprise Content Management platform and also the Documentum D2 application providing setup and implementation of the intuitive interface, implementation and migration. The technology of configuration management D2 supports maintaining magazines of audit, creation of reports and electronic signatures for ensuring compliance to requirements of regulators, services of management of lifecycle and managements of documentation and also special opportunities for Life Sciences industry.

Specific Features

• IT management simplification. Thanks to existence of flexible functionality of lifecycles of the document, joint work process automation, enhanced capabilities of a configuration and creation of convenient user environment, the IT personnel of the company user will be concentrated on innovations and projects, important for business, but not on technical issues.

• Economy. Replacement of internal development with simple setup of a configuration of applications allows to leave from need of programming, to reduce costs for commissioning. These measures will allow to reduce total cost of ownership by 20% sensitively.

• Quality improvement of processes and interaction. The unified architecture constructed on the basis of the reference DIA EDM model provides mutual compliance of processes, a possibility of collective creation of documents, management of documents, both in the organization, and beyond its limits. At the same time such areas as research and development, production and quality, clinical developments, the contract/clinical research organizations can be covered.

• Compliance to requirements of regulators. The automated execution the politician, the reporting, support of the electronic signature, maintaining magazines of audit provide compliance to requirements of world regulators and to industry standards, such as FDA of 21 CFR Part 11, GxP, as well as reference TMF models.