Clinical Trials in France

Clinical trials in Spain. Selecting European countries for conducting your clinical trial

Date & Time: 10 December 2024 from 11:00 AM to 12:30 PM (CET)

Overview
In this webinar, we will take you to the heart of French excellence as we explore the clinical research landscape in France and explain how this pioneering nation has become a leading global player.
We will cover a broad range of topics related to both medicinal products and medical devices, including:

• Key figures and statistics in clinical research
• Patient recruitment potential in France, with a focus on specific populations
• Regulatory and ethical approval processes
• Overview of the French clinical research ecosystem, including access to CROs, service providers, and vendors (from early to late phase)
• Acceptability and evolution of decentralized trial methods
• Cost considerations

We will conclude with key insights that highlight why France is a unique and strategic location for conducting clinical trials.

Presenters:

Laëtitia Gidelle

Laëtitia Gidelle is an accomplished leader in the clinical trial sector, having built the PSI French entity from the ground up. With 25 years of experience, she possesses a profound understanding of clinical trials and contract research organizations (CROs), paired with strong leadership abilities.

One of the guiding principles at PSI is "Every Patient Counts," a mantra that Laëtitia has embraced as her personal mission. Driven by a profound passion for expanding patient access to innovative treatments, she recognizes that clinical trials are essential not only for enhancing patient care but also for equipping hospitals with a range of therapeutic options. Laëtitia's dedication extends beyond her organization; she and her team actively engage in various task forces within AFCRO, reflecting her commitment to advancing the clinical trial landscape for the benefit of all.

Outside of her professional endeavors, Laëtitia enjoys gardening, cooking, and creating lasting memories with her family and friends.

Christophe Clément

Christophe Clément has been Business Development Director at ICTA since January 2020.

He holds a Master II in Physiology and Physiopathology of the Respiratory System, a diploma from CESAM (Statistical methodologies applied to Clinical Research) and a level D diploma in Project Management.

Christophe joined ICTA in 1995 where he rose through the ranks, first as a clinical research associate and then as project manager, also responsible for coordinating oncology and international projects, before becoming Head of International Clinical Operations for 10 years.

Since January 2020, he has been Director of Business Development, focusing on Biotech and Medtech development activities to propose strategic plans approach for early phases of development.

Anne Péron

Anne Péron is the Vice President of Business Development and Director of Marketing at Biotrial.

With extensive experience in business development and marketing, she has held various leadership roles in the pharmaceutical and clinical research industries, managing strategic relationships, sales, and marketing teams. Anne previously worked at Harvard Apparatus and holds an Advanced master’s in marketing research and Decision Making from NEOMA Business School, along with a postgraduate degree in Neuropharmacology from Université de Bordeaux.

Anne joined Biotrial 20 years ago and has led the global sales team since November 2018, helping pharma and biotech companies access comprehensive solutions from non-clinical to full-package clinical services, including phase 1 studies. Guided by Biotrial’s core values of innovation, quality, transparency, and commitment, her leadership supports the company's mission to advance drug development and improve patient care.

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Host or Publisher EUCROF