Configuration Control vs. Document Control – Managing Design Changes Across Modern Quality Systems
Learn why Configuration Architecture — not Document Control — defines the modern Quality System, and how treating relationships as first-class objects strengthens traceability, change control, and inspection readiness.
Instructor
José Mora
Medical Device Quality Systems & Configuration Management Consultant
What You'll Learn
About This Event
Curriculum
Requirements
- Quality Assurance, Regulatory Affairs, Design/Development, Systems/Software, and Manufacturing Engineering professionals
- Applicable to Configuration/Change Management, Document/Records Management, Risk Management, Verification/Validation, and Supplier Quality roles
- Relevant to PLM, MES, ERP, and Digital Transformation teams, and executive leaders responsible for Quality System effectiveness
Who Should Attend
The primary audience includes managers, engineers, auditors, consultants, and technical professionals who need to understand how configuration decisions affect product quality, regulatory evidence, manufacturing execution, and change control. The webinar is particularly relevant to professionals who manage large document sets, investigate inconsistencies, conduct change assessments, support inspections, or evaluate digital Quality System investments. It is also designed for leaders who need a coherent foundation for PLM, Digital Thread, Digital Twin, connected manufacturing, Model-Based Engineering, and AI-enabled Quality Systems — including Quality Assurance and Quality Engineering, Regulatory Affairs, Design and Development Engineering, Systems and Software Engineering, Manufacturing and Process Engineering, Configuration and Change Management, Document and Records Management, Risk Management, Verification and Validation, Supplier Quality, Operations and Technical Training, PLM/MES/ERP and Digital Transformation teams, and executive leaders responsible for Quality System effectiveness.
Areas Covered
Meet Your Instructor

José Mora
Medical Device Quality Systems & Configuration Management Consultant
José Ignacio Mora is a Principal Consultant specializing in Manufacturing Engineering, Quality Systems, Design Controls, and Configuration Management within the medical device industry. For more than three decades he has worked across product development, manufacturing, quality systems, process validation, supplier management, technology transfer, and regulatory compliance. His experience includes leadership positions at Boston Scientific, Stryker Orthopedics, Cordis Corporation, and multiple start-up medical device organizations. José is the creator of the Lean Documents and Lean Configuration methodology, a relationship-centric approach to managing quality system information. His work focuses on improving traceability, reducing information fragmentation, strengthening inspection readiness, and creating more effective connections between requirements, risks, verification activities, validation activities, and released product configurations. Drawing from practical experience in design controls, process validation, manufacturing systems, quality systems remediation, and organizational transformation, José provides a unique perspective on how organizations can achieve compliance while simultaneously reducing complexity and improving operational effectiveness.
Event Details
Format
Live Webinar
Duration
1.5 hours
Certificate
Included
Date
Monday, August 31, 2026
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