Pharmaceutical & Life Sciences

Achieve compliant management of all electronic records and documents

OpenText ECM applications for Life Sciences are designed to address the complete lifecycle of all content within a pharmaceutical, biotechnology or medical device manufacturing company. OpenText’s strength in life sciences is their ability to deliver best-of-breed vertical market solutions which provide 21 CFR Part 11 compliance on one of the top Enterprise Content Management suites in the market.

OpenText ECM applications for Life Sciences provides product flexibility, which in turn allows customers to address multiple business processes through configuration – rather than programming – and does not restrict the use of the system to a predefined set of interfaces, templates, appearances and processes. Organizations can address many business process challenges using OpenText technology. Some of these processes include SOP management, regulatory submissions management, CAPA management and product development lifecycle. In addition, life sciences companies can leverage OpenText’s market leading solutions for contracts management, eDiscovery, ERP data and document archiving, accounts payable, web content management and digital asset management.

OpenText ECM Applications for Pharmaceutical & Life Sciences

OpenText ECM applications for Pharmaceutical & Life Sciences include:

  • OpenText Regulated Documents is a complete solution to securely manage key documents throughout a controlled lifecycle in compliance with relevant regulatory requirements.
  • OpenText Quality Management is a complete solution for businesses operating in highly regulated industries that helps to ensure quality regulatory compliance in their products and services.
  • OpenText Clinicals is designed to manage the capture and review of all trial-related information throughout the setup, conduct and review of clinical trials.
  • OpenText Collaborative Submissions is a comprehensive, collaborative environment for the authoring, review, approval, assembly, export, and long-term management of all regulatory documents and submissions.