Vaccines and Clinical Testing: Strategic Entry into Trials in Europe

Biotech, Clinical Trials, Drug Discovery & Development, Life Science, Pharma, Pharmaceutical Regulation,
  • Monday, July 28, 2025 | 9:30am EDT (NA) / 2:30pm BST (UK) / 3:30pm CEST (EU-Central)
  • 60 min

Early-stage vaccine developers face critical decisions: where to conduct trials, how to navigate various regulatory systems and how to generate the evidence needed to proceed swiftly and with scientific integrity.

This webinar is designed for biotech innovators, NGOs and pharma teams preparing to bring their vaccine candidates into clinical testing. This session will provide clear, practical insight into how Europe can support more innovative early development, from identifying the right countries and sites to using epidemiological evidence to shape compelling clinical strategies.

Real-world examples will be discussed, including Belgium’s infrastructure for early-phase and human challenge studies. The webinar will also outline alternative pathways that can reduce risk, optimize timelines and help assets reach their next milestone.

Register for this webinar to learn how to make confident, informed decisions, supported by a partner with deep regional expertise and end-to-end capabilities in vaccines and clinical testing, including infectious disease research.

Speakers

Laurence De Moerlooze, P95

Laurence De Moerlooze, Chief Medical Officer, P95

Laurence is currently the Chief Medical Officer at P95, bringing a wealth of expertise and leadership to P95’s management team, shaped by an impressive career marked by pivotal positions, including Executive Vice President and Chief Medical Officer at Bavarian Nordic, and influential senior roles at Takeda and GSK. After earning a PhD in Virology from the University of Liège and undertaking extensive postdoctoral work in Montreal, London and Brussels, Laurence amassed over 15 years at GSK Biologicals. During this time, she was at the forefront of regulatory affairs, vaccine development leadership and medical affairs, playing a significant role in developing vaccines, including one for HPV. Her subsequent leadership roles extended to the development of vaccines for Zika and norovirus as Vice President at Takeda, followed by a 4-year tenure as Chief Medical Officer at Bavarian Nordic.

Message Presenter
Pierre Van Damme, Vaccinopolis

Pierre Van Damme, Director, Vaccinopolis

Professor Dr. Pierre Van Damme, a prominent figure in vaccinology, obtained his MD and PhD from the University of Antwerp and has been active in vaccine research for over 35 years. He has been a full professor at the University of Antwerp since 2000. He is the founder and director of the Centre for the Evaluation of Vaccination (CEV), a WHO Collaborating Centre. Under his leadership, the CEV has conducted over 500 vaccine trials, including a notable oral polio vaccine trial for the Gates Foundation. In 2022, he launched Vaccinopolis for advanced vaccine trials. He has authored over 550 peer-reviewed papers and received several awards.

Message Presenter
Kaatje Bollaerts, P95

Kaatje Bollaerts, Epidemiology Business Head, P95

Kaatje Bollaerts is the Epidemiology Business Head at P95, where she oversees the design, execution and strategy of global epidemiological research focused on vaccines and infectious diseases. With over 18 years of experience and a PhD in Biostatistics from Hasselt University, she has led major public-private initiatives, including ADVANCE, DRIVE, VITAL, COVIDRIVE and id.DRIVE. Before joining P95 in 2013, she held research roles at Sciensano and KU Leuven, contributing to national public health efforts. Kaatje is widely recognized for her scientific leadership, collaborative approach and commitment to translating data into meaningful public health insights.

Message Presenter
Eleni Koursari, P95

(Moderator) Eleni Koursari, Marketing and Communications Manager, P95

Eleni Koursari is a trained microbiologist with hands-on experience in molecular virology and infectious disease research. Building on her scientific background, she transitioned into communication and marketing roles across non-profit and research organizations in the public health arena. She is currently the Marketing and Communications Manager at P95, leading global marketing initiatives.

Message Presenter

Who Should Attend?

This webinar will appeal to the following professionals and organizations:

  • Biotech founders, regulatory leads and clinical directors preparing for first-in-human or early-phase vaccine trials
  • NGOs and public-private partnerships advancing vaccine candidates toward proof-of-concept
  • Pharma teams planning Phase I–II trials in Europe and seeking flexible execution models
  • Regulatory and clinical operations professionals evaluating country strategies
  • Decision-makers looking to de-risk development through evidence-based planning
  • Clinical trial managers interested in practical insights on early-phase trial delivery

What You Will Learn

Attendees will gain insight into:

  • How epidemiology strengthens early clinical strategy and supports regulatory success
  • What makes Europe, using Belgium as an example, a wise choice for vaccine trials
  • When and why to consider alternative trial models like adaptive design or human challenge studies
  • How clinical endpoints likely predicting efficacy have been used to support vaccine licensure
  • Common pitfalls in early vaccine development and how to avoid them
  • How P95 supports clients across planning, regulatory navigation and trial execution
  • Practical tips to speed up timelines while maintaining data quality and operational excellence

Xtalks Partner

P95 

P95 is a leading global provider of epidemiology and clinical solutions with a specialty focus on vaccines and infectious diseases. Headquartered in Belgium, P95 has regional hub offices in Africa (South Africa), Latin America (Colombia), North America (USA) and Southeast Asia (Thailand). P95’s full-service CRO solutions span 5 continents, with 300 staff and experience across 30 countries. With over 25 years of experience, P95 is dedicated to delivering flexible, customer-centrical solutions, powered by a team passionate about driving positive change in global health.

P95’s range of high-quality services include:

  • Clinical Trials Phase I-IV
  • Epidemiology and RWE
  • Vaccine Development Consulting
  • Study Start-up and Regulatory
  • Clinical Monitoring
  • Home Nursing
  • Sample Management
  • Medical Monitoring
  • Pharmacovigilance
  • Data Management
  • Biostatistics
  • Medical Writing
  • Qualitative Research

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