A practical approach to deploying, validating, and maintaining your eQMS in regulated environments.
Deploying an electronic Quality Management System (eQMS) in a regulated environment should not mean months of implementation complexity, excessive validation effort, or uncertainty about ongoing compliance.
Join Dr. Boris Lutz, CEO and Founder of BPA Solutions, and Valarie King Baley, CEO of OnShore Technology Group, for a practical webinar on how medical device and life sciences organizations can accelerate eQMS deployment while maintaining a risk-based approach to computer system validation.
Discover how BPAMedical365, a validation-ready eQMS built on Microsoft 365, combines preconfigured quality processes and validation documentation with OnShore’s digital validation capabilities and risk-based methodology. Together, these approaches help organizations streamline implementation, focus testing on what matters most, and establish the evidence needed to support their validated state.
Through a live demonstration, see how quality workflows connect from nonconformance and investigation to CAPA, document control, and training. Explore electronic signatures, audit trails, validation documentation, risk assessments, traceability, and the path from validation readiness to a validated system.
Register now if you are seeking a more efficient validation approach
Webinar recording will be made available to all registered participants
KEY HIGHLIGHTS
- Accelerate eQMS deployment: Discover how preconfigured quality workflows and Microsoft 365 integration can simplify implementation and speed up time to value.
- Make validation more efficient: Learn how validation documentation, risk assessments, and risk-based testing aligned with FDA Computer Software Assurance (CSA) principles can help focus effort where it matters most.
- Move from validation-ready to validated: Understand how to establish a validated baseline, generate objective evidence, and define your organization’s validation responsibilities.
- See the approach in action: Follow a live quality scenario from nonconformance through investigation, CAPA, document control, and training.
