Chemical Analysis: The Essential Tool for Controlling Toxicological Risks – Webinar

21/01/2026

    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.

    • Date: 21/01/2026
    • End date: 21/01/2026
    • Type of event: Live Stream
    • Time: 11:00 AM (CET)
    • Language: English
    • Registration link: https://bit.ly/4aojj0P

    Key Topics 

    • The role of chemical analysis in biocompatibility evaluation 
    • Main stages of chemical analysis (extraction, identification, quantification) 
    • How to interpret GC-MS and LC-MS results 
    • Linking detected compounds to materials and processes 
    • Avoiding false positives and improving analytical accuracy 
    • How specific molecule analysis helps reduce toxicological uncertainty 

     

    Who Should Attend 

    This webinar is intended for professionals involved in:   

    • Medical device design and validation 
    • Regulatory affairs and toxicology 
    • Quality assurance and R&D 
    • Material and process engineering 
    SPEAKERS

    Speakers 

    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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