Healixia Clinical Conference 2026
Join us for a full day - including lunch, coffee breaks and networking reception - where we touch upon different 'hot topics' in Clinical Research.
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Aneta Tyszkiewicz
Aneta is Director, Science & Regulatory at the European Federation of Pharmaceutical Industries and Associations (EFPIA), representing the R&D-based pharmaceutical industry in Europe. She leads EFPIA’s policy and advocacy on data, real-world evidence, and emerging technologies, including biotechnologies.
Her work focuses on advancing the digital transformation of healthcare in Europe to enable the development of innovative, trusted solutions that deliver tangible benefits for patients.
Aneta previously held roles at the Council of European Dentists, the International Diabetes Federation, and in consulting.
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Anne Lenaers
Anne Lenaers is a pharmacist and regulatory expert at the Belgian Federal Agency for Medicines and Health Products (FAMHP/AFMPS). Working within the R&D Division of DG PRE, she acts as Belgium's National Contact Point for the Clinical Trials Regulation (CTR) and contributes to European regulatory collaboration as a member of the Clinical Trials Coordination Group (CTCG).
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Christophe Deben
Professor Tumor Biology and Organoids | Group Leader Tumoroid Screening Lab | Head DrugVision.AI Screening Platform and UZA/UAntwerp Tumor Organoid Biobank | Co-founder Orbits Oncology and Sightera Biosciences
As head of the Tumoroid Screening lab at the University of Antwerp, I combine my passion for cancer research with my interest in new technologies to develop more advanced 3D cancer models and automated drug screening assays.
My team applies a multidisciplinary approach that combines cancer biology, live-cell imaging, and data science to find new combination strategies that target cancer cells more efficiently and to improve the prediction of a clinical response from ex vivo tumoroid drug screenings. In addition, we offer proprietary drug screenings assays to academic and industry partners using our own patient-derived tumoroid biobank.
As co-founder of Orbits Oncology, my goal is to make advanced live-cell image analysis more accessible to academic researchers and facilitate the implementation of patient-derived tumoroid models to support the next breakthroughs in cancer research. For industry, we can develop custom solutions for live-cell image data management and compression, image analysis and downstream data visualisation. More info on www.orbits-oncology.com. -
Denis Lacombe
Denis Lacombe graduated with his MD from the University of Marseilles (France) in 1988 and obtained a Master Post-Doctoral Fellowship at The Roswell Park Cancer Institute (Buffalo, NY USA) for research in pharmacology and pharmacokinetics from 1989 to 1991. From 1991 to 1993, he worked as a Clinical Research Advisor in charge of the development of a new drug in oncology in the pharmaceutical industry.
Dr Lacombe joined the EORTC in 1993 as a research fellow and quickly became a very active and productive Clinical Research Physician involved in the conduct of clinical research from protocol development through publication for a number of oncology indications from phase I to phase III. Dr Lacombe contributed to the strategic evolution of the EORTC pan-European clinical and translational research infrastructure as well as developing partnerships with multiple stakeholders.
Dr Lacombe rose to the position of Director EORTC Headquarters in 2010, was appointed Director General in April 2015 and Chief Executive Officer in June 2021. In his current position, Denis Lacombe leads all activities promoting the EORTC as a major European organization in Cancer Clinical and Translational Research, including scientific activities, public relations and medium-term strategies as defined by the EORTC Board as well as internal and external communications. -
Dirk Meyssen
Dirk Meyssen is Senior Manager Clinical Operations at Johnson & Johnson, leading clinical operations teams across Belgium and the Netherlands. Having worked in clinical research from site level through trial management and leadership roles, Dirk has witnessed firsthand how the clinical trial landscape in Belgium has evolved over the past decade. Today, he is passionate about strengthening Belgium's position as a leading research country by improving study start-up, accelerating trial delivery, and developing high-performing teams that put people, patients, and sites at the center of clinical research.
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Frank Van Gelder
Frank is a senior strategist at the intersection of global healthcare, life sciences supply chains, and academic research,
with a career spanning more than three decades. His work focuses on strengthening critical pharmaceutical and MedTech
supply chains, integrating digital and AI-driven health applications, and advancing education at the nexus of industry and
academia.
He began his career in 1989 in critical patient care at one of Europe’s largest university hospitals, where he developed deep
expertise in organ, tissue, and cell transplantation, as well as intensive care medicine. This clinical foundation continues to
inform his strategic perspective on healthcare systems and precision therapy logistics.
Over the past 15 years, Frank has emerged as a leading voice in life sciences supply chain strategy, with a particular
emphasis on resilient, high-quality, and sustainable pharmaceutical logistics. His work increasingly addresses global
vulnerabilities, geopolitical disruptions, and the transformation of supply networks that underpin access to essential and
life-saving therapies.
A prolific academic contributor, Frank has authored more than 250 peer-reviewed scientific publications and over 30
international industry white papers. He is a frequent keynote speaker and commentator, with more than 400 international
lectures and regular contributions to global media on healthcare and supply chain resilience. His academic engagement is
further reflected in his ongoing pursuit of advanced studies and research both in medical and supply chain research.
Frank holds several executive and academic appointments. He is actively involved in teaching and program development at
the University of Antwerp and serves on the business faculty of Antwerp Management School and Thomas More University
of Applied Sciences. He is a board member of the Advisory Board on Global Supply Chain at Antwerp Management School
and contributes to the at.las ATMP Supply Chain Excellence Centre. He is also co-founder and program co-director of the
International Pharma Logistics Masterclass, “Where Business Meets Academics” and the Pharma Logistics Winter
University, both designed to bridge strategic industry insights with academic rigor.
Beyond his professional work, Frank draws inspiration from astronomy and astrophysics, pursuits he actively studies
alongside outdoor activities such as mountain biking and culinary exploration. He is a strong advocate for interdisciplinary
thinking, diversity of perspectives, and the role of implementation science and knowledge-sharing as catalysts for
meaningful innovation and sustainable development.
CEO, Mediconed Consultancy
Secretary General Pharma.Aero
Member of the Advisory Board of Global Supply Chain AMS
Faculty Antwerp Management School and University of Antwerp
Faculty University of Applied Sciences Leuven and Thomas More Academy -
Ingrid Klingmann
Chairman at EFGCP, President at EUFEMED, Vice-President at PharmaTrain Federation asbl, Managing Director at Pharmaplex bv
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Jade Verrept
Jade Verrept is Program Manager at the Provincial Development Authority Antwerp, as well as co-founder of the Antwerp ATMP ecosystem at.las. Jade is responsible for advancing the province’s regional innovation agenda, focusing on new technologies in life sciences and logistics. Her focus is both on the development of innovation campuses, and on the creation of dynamic innovation clusters.
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Kathy Plachytka
Kathy Plachytka, MSc, is an independent Clinical Research Consultant and experienced clinical research professional with over 12 years of experience across both CRO and pharmaceutical environments.
She started her career at Quintiles, now IQVIA R&DS, in 2014, progressing from Regulatory & Start-up Coordinator to Clinical Research Associate and Senior Clinical Research Associate. During her time at IQVIA, she gained extensive experience across the clinical trial lifecycle, including study start-up, site selection, initiation, monitoring, close-out and site management, across therapeutic areas including oncology, neurology, rare diseases, paediatrics and IBD.
Since 2021, Kathy has worked as an independent Clinical Research Consultant, providing clinical research expertise across pharmaceutical and CRO environments. Since 2023, she has supported AstraZeneca as a Senior Clinical Research Associate, with a primary focus on oncology and hands-on involvement across a range of clinical trials and study activities.
Combining strong hands-on CRA expertise with both CRO and pharmaceutical perspectives, Kathy brings a practical, site-focused approach to clinical trial delivery, with a strong focus on quality, patient safety, collaboration and efficient study execution.
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Katrien Asnong
Katrien Asnong graduated with a Master of Science in Nursing from the Catholic University of Leuven in 2000, after obtaining her bachelor's degree in nursing in 1997. She began her career as a research nurse in the IBD unit of Professor Rutgeerts at University Hospitals Leuven, where she gained extensive experience in the care of patients with inflammatory bowel disease (IBD) and in clinical research. After five years, she moved to the private sector, where she worked as a Clinical Research Associate (CRA) and later as a Clinical Project Leader in the medical device industry. However, missing direct patient contact and hands-on clinical work, she decided to return to IBD care. In 2014, she joined the IBD Clinic of Dr. Bossuyt at Imelda Hospital in Bonheiden. There, she coordinates clinical trials in Crohn's disease and ulcerative colitis as part of the clinical research nursing team. Katrien has been a member of BINAstoria, the Belgian professional association for healthcare professionals involved in the care of patients with inflammatory bowel disease (IBD), since June 2019. She served on its board from November 2019 to 2021. Since 2024, she has been teaching the course Introduction to Clinical Trials in the PXL Next postgraduate IMID programme. In 2026, she obtained her qualification as a Nurse Specialist. Katrien is a member of the European Crohn's and Colitis Organisation (ECCO) and has been an invited speaker at the ECCO Congress on multiple occasions.
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Katrien Tartaglia
Passionate about clinical research and the power of collaboration. As Head of the Clinical Trial Unit at Future Health, she is committed to connecting researchers, healthcare professionals, industry partners, and fellow hospitals to strengthen the clinical research landscape in Belgium. Through efficient processes, knowledge sharing, and team development, she supports the sustainable delivery of high-quality clinical studies. -
Lauren Swinnen
Lauren Swinnen is a Clinical Project Manager and Regulatory & Safety Specialist at Archer Research, where she manages European device studies across different therapeutic areas from start-up through close-out. She holds a PhD in Biomedical Sciences from KU Leuven, where her research focused on a wearable device for long-term epileptic seizure monitoring. Lauren combines hands-on clinical operations experience with regulatory and safety expertise under EU MDR 2017/745, ISO 14155, and GCP.
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Mieke Tempels
Director of Operations with extensive experience leading clinical and operational programs within the medical device CRO industry. Passionate about building high-performing teams, optimizing processes, and delivering efficient, compliant solutions that support innovation in healthcare. Focused on operational excellence, strategic growth, and strong client partnerships across complex clinical environments.
15+ years experience in clinical trials.
Background in Biomedical and Pharmaceutical Sciences at the University of Hasselt, Liège and Leuven, Belgium.
Archer Research is a CRO specialized in clinical studies with medical devices. Helped the company and the team grow to where we are today. A valued company, setting up and managing clinical studies in Europe, supporting our clients from clinical evaluation to clinical investigation. -
Peter Bossuyt
Dr Bossuyt studied medicine at the Catholic University of Leuven, Belgium, and graduated magna cum laude in 2004. He pursued his GI fellowship in several hospitals in Belgium and at UZ Leuven. After completing his GI fellowship in 2009, he took up a fellowship in advanced endoscopy at the Academic Medical Centre, Amsterdam. Between 2010 and 2015 he was a consulting staff member at the University Hospitals of Leuven. He obtained a PhD entitled “Value of endoscopic scoring and imaging for the prognosis and follow up of IBD” at the University of Leuven in 2021. His research focuses on clinical and strategic trials in IBD and the definitions of endoscopic and imaging targets in IBD. His clinical works focuses on e-health tools in IBD and quality improvement projects.
He is currently international principal investigator of 3 clinical trials in IBD and endoscopy. He is an editorial board member of the Journal of Crohn’s and Colitis, past-president of the Belgian IBD Research and Development Group, past-board member of ECCO’s Clinical Research Committee, ClinCom and past-board member of the Belgian society of gastrointestinal endoscopy, BSGIE. He won the Belgian IBD research price in 2011, 2021 and 2025, the ESGE Innovation of the year award in 2018 and the ECCO IIS award in 2025. He published over 150 peer-reviewed articles in the NEJM, Lancet, JAMA, Gastroenterology, Gut, Lancet Gastroenterology and Hepatology, JCC among others (H-index 48).
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Thomas Van der Plaetsen
Thomas is a former professional decathlete. He became the 2016 European Champion only 2 years after a testicular cancer treatment and is a two-time Olympian. Through his foundation "Back on track" he helped people get fit again after their cancer treatment. He now coaches up and coming track and field athletes and aims to inspire people with his story.
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Virginie Barthel
Virginie Barthel has more than 19 years of clinical research experience, from CRA to Clinical Operations leadership in biotech environments. Specializing in early-phase development, she provides her expertise to early-stage biotechs to ensure a strong start in clinical development and treat the first patients. Her cross-functional expertise drives efficient, patient-focused clinical operations, creating lasting value for these companies.