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.
In collaboration with
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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.
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.
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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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Regulatory, quality, and clinical support for MedTech startups and scale-ups bringing innovative devices to market.
