Live WEBINAR - DECEMBER 7, 2022 @ 2PM ET
Live Demo of Adept for Life Sciences
Life Sciences companies require centralized access and control of GxP documents and CAD drawings to improve quality processes and simplify compliance and system validation for FDA 21-CFR Part 11 and EMA Volume 4, Annex 11.
Join us and gain insights to align your teams on a centralized source of truth, simplify document access, automate workflow, provide an extensive audit trail, and maintain regulatory compliance.
Discover how engineering document management and system validation services can help you:
- lower the cost and effort of compliance and validation
- reduce risk of noncompliance with streamlined audits
- Eliminate costly mistakes and safety issues
- Simplify collaboration and accelerate projects
A live Q &A session will follow the presentation.