WEBINAR REPLAY

Engineering Document Management for Simplified Compliance & Validation

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 Merck, IPS, and Synergis Software to learn how Merck is leveraging the Synergis Adept platform to address these issues while driving standards and best practices.

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

You will 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.