Chemical analysis plays a crucial role in ensuring the safety and compliance of medical devices. With the latest updates to ISO 10993-1 (2025) and the Medical Devices Regulation (MDR 2017/745), understanding how to interpret analytical data has become essential to control toxicological risks and guarantee biocompatibility.
In this webinar, our experts will guide you through how chemical characterization supports the biological evaluation strategy, from data generation to regulatory argumentation.
This webinar is intended for professionals involved in:
Both speakers bring extensive experience in analytical chemistry and regulatory compliance for medical devices.
Marilys Blanchy – Expert in material and chemical analysis at Applus+ Laboratories
Expert in material and chemical analysis at Applus+ Laboratories, where she focuses on the characterization and qualification of materials to support product safety, performance, and regulatory compliance in demanding industrial sectors. In her role, she applies advanced analytical techniques to study the composition, structure, and behavior of polymers, coatings, adhesives, and other non-metallic materials, and translates complex physico-chemical data into clear, actionable conclusions for manufacturers and design teams.
Emilie Danel – Senior Project Manager at Applus+ Laboratories
Senior Project Manager at Applus+ Laboratories, where she leads complex testing and engineering projects to support clients in bringing safe, reliable, and compliant products to market. She coordinates multidisciplinary teams, manages project scope, schedule, and budget, and serves as a key interface with customers to align technical deliverables with business and regulatory requirements. With extensive experience in laboratory services and applied testing, she helps structure innovative, high‑value projects that strengthen Applus+ Laboratories’ role as a trusted partner in product development and qualification.
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