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Gevers & QbD Group roadshow

Event for Biotech and medtech firms

Gevers and QbD Group, partners in life sciences and healthcare industries, bring you an exclusive roadshow. Drawing on their expertise, they’ll share practical insights, expert tips, and real-world examples to help Biotech and MedTech companies overcome common challenges, seize opportunities for early company value increases, and accelerate market entry. This is an event you don’t want to miss! Join us to gain valuable knowledge specifically tailored for Biotech and MedTech firms. 

The next date of our roadshow:


Liège – LégiaPark in CA Room

25th September 2025 at 12 PM

Meet our attending experts:


Stijn Lagaert (Gevers)
 
Stijn is an expert in biotechnology, pharmaceutical chemistry and various other technologies. Specialized in European and international patent applications, he is a recognized authority on Supplementary Protection Certificates and patent litigation in Belgium. See him at our biotech and medtech event.
 
Emilie Logie (Gevers)
 
Emilie specializes in life sciences and transitioned from research to patent engineering. She advises companies on patent strategy and drafts and prosecutes European and international patent applications.

Anne-Sophie Grell (QbD Group) 
 
Anne-Sophie is a regulatory and quality affairs specialist with expertise in MDR compliance, international medical device regulations, and CE marking requirements. She combines extensive experience with technical knowledge and will be sharing her insights at the biotech and medtech event.
 

Kirsten Van Garsse (QbD Group) 
 
Kirsten Van Garsse obtained her Master’s degree in Biomedical Sciences in 2002 from the Vrije Universiteit Brussel (VUB) and has amassed extensive experience in the In Vitro Diagnostic Medical Device Industry. She joined Qarad, now part of the QbD Group, a consulting company specialized in Regulatory Affairs and Quality Systems for the IVD and Medical Device industry, at the end of 2017.

In her role as Director of Authorized Representative Services & Manager of IVD Regulatory Affairs, Kirsten applies her wealth of experience to Regulatory Affairs projects, adeptly translating regulations into compliant business processes and applications. Additionally, she oversees the various Representation Services offered by Qarad, ensuring clients receive expert support in navigating regulatory requirements.

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