ENOVIA for Life Sciences Industry

When companies were questioned as part of a recent AMR Research study, 31 percent of U.S. respondents identified product quality as one of the top reasons why product launches fail, while 20 percent also highlighted regulatory issues as being a key factor.

Adaptive Corporation, in partnership with Dassault Systèmes, introduces the ENOVIA platform which offers customers a single, flexible solution with integrated business processes to better manage core intellectual property. Based on a service oriented architecture (SOA), the Life Science Accelerator facilitates seamless interaction between all ENOVIA-based business processes including Corrective and Preventive Actions (CAPA), Product Complaints, Change Control, Product Development and Supplier Control.

“After years of working with some of the world’s leading life sciences companies, we are developing a series of products that leverage best practices to better serve specific industry needs,” said Mickey Garcia, director of Life Sciences Industry Strategy, ENOVIA, Dassault Systèmes. “Our customers – both pharmaceutical and medical device manufacturers – rely on ENOVIA solutions as central tools for managing product quality, promoting greater supply chain collaboration, and ensuring regulatory compliance.” 

ENOVIA Life Sciences Accelerator for Quality Issues

The ENOVIA Life Sciences Accelerator for Quality Issues provides a flexible, ready-to-use business process for the management of Quality Issues such as CAPAs and Product Complaints. The Accelerator enables customers to automate many of the routine aspects of quality investigations, reducing waste and focusing attention on the truly critical issues of risk, root cause and remediation. This product also helps customers to verify that the quality investigation is executed properly and that all required deliverables are completed resulting in lower regulatory risk.

ENOVIA Life Sciences Accelerator for Change Control 

The ENOVIA Life Sciences Accelerator for Change Control also provides a ready-to-use business process for the management of changes to regulated documents, procedures and specifications throughout an organization. Delivering a single, robust Change Control process, it improves the speed of changes and reduces errors introduced by manual handoffs. This approach is designed to help customers reduce regulatory risk by automatically enforcing critical process steps, guiding regulatory, safety and financial impact assessments and capturing Part 11-compliant signatures based on a company-defined approval matrix.