Medical Device Validation Solutions for Evolving Industry Needs

The rapid expansion of computer systems in medical device manufacturing is driving an urgent need for modernized validation approaches. This webinar prepares medical device leaders for the validation landscape of 2026 and beyond, with practical guidance on adopting digital validation in a CSA-aligned, risk-based framework. Kathianne Ross, Manager of IT Compliance at Fujirebio Diagnostics, and Kneat Senior Customer Success Manager Tim Akin bring deep expertise in FDA 21 CFR Part 11, GAMP methodology, and medical device compliance. Together they explore how digital validation builds confidence while eliminating redundant activities, why CSA demands a rethink of traditional medical device validation, and what leaders need to plan for when making the transition. Whether preparing for a new system deployment, responding to regulatory pressure, or building a more scalable validation program, this webinar delivers the strategic clarity and practical direction you need. Watch on demand now and ensure your medical device organization is ready for the validation demands of 2026 with Kneat Gx.