QbD Group
    On Demand Webinar

    From R&D to market: IP and regulatory strategy across the product life cycle

    This webinar follows the stages of a product’s life cycle, explaining how structured, science-based development and intellectual property considerations support regulatory alignment and long-term value creation.

    On Demand
    60 min
    Regulatory Affairs · Life Sciences
    English

    In collaboration with

    Biovia and Gevers

    What you'll learn

    • How to manage a product strategically throughout its full life cycle
    • The role of Quality by Design in development and regulatory pathways
    • How IP and regulatory strategies interact across product stages
    • Practical insights from real-life industry cases

    Learn from the best

    Speakers

    Anne-Sophie Grell

    Anne-Sophie Grell

    Business Unit Manager RA Medical Devices at QbD Group

    Anne-Sophie is a Regulatory Affairs leader with over two decades of experience in medical physics, diagnostic imaging, and medical device regulation. She supports clients navigating EU MDR, FDA, and international regulatory frameworks.

    Stijn Lagaert

    Stijn Lagaert

    European and Belgian Patent, AttorneyEuropean Patent Litigator and Partner at Gevers

    Stijn Lagaert possesses extensive expertise spanning the biotechnology, pharmaceutical chemistry, plant protection products, fertilizers, and food and feed technologies sectors. He is well-versed in the entire spectrum of patent-related activities, including the meticulous drafting and prosecution of patents. As a European and Belgian Patent Attorney and European Patent Litigator, he brings deep IP knowledge to the life sciences industry.

    Register here

    Is this for you?

    Who should attend?

    This webinar targets R&D-driven organizations and professionals responsible for development strategy, quality by design implementation, and regulatory alignment across the product life cycle. We look forward to welcoming you to this insightful session!

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