Contribution of Methodologies Adapted to Clinical Trials Focusing on High Risk Medical Devices. - C. Vidal; R. Beuscart; Thierry Chevallier (BIODEVICES, 2020)

Threats and Opportunities for the Clinical Investigation of High-risk Medical Devices in the Context of the New European Regulations. - Lionel Pazart; Sylvia Pelayo; Thierry Chevallier; Gabriel Gruionu; Philippe Mabo; Yves Bayon; Frédéric Barbot; Thomas Lihoreau; Catherine Roussel; Nicos Maglaveras; Eirini Lekka; Hugo Alexandre Ferreira; et al. (BIODEVICES, 2021)

Combined Medical Devices: Which Classification for These Borderline Products and Which Consequences for the Manufacturers - About a Use Case in Skin Healing Area. - Anaïs Vaissière; Thierry Chevallier (BIODEVICES, 2022)

The Role of Massive Databases in the Post-market Clinical Follow-up of Medical Devices. - Marion Burland; Thierry Chevallier (BIODEVICES, 2022)

Post-market Clinical Follow-up (PMCF) GAP Analysis for Legacy Devices Class III between the Medical Device Directive (MDD 93/42/EEC) and the Medical Device Regulation (MDR 2017/745). - Marina Makeenko; Thierry Chevallier (BIODEVICES, 2022)

Medical Devices Used in Extreme Conditions in Pre-Hospital Emergency Medicine: Overview of the Issue, Use Case Regarding Mechanical Ventilation at Altitude and Advice. - Carine Malle; Alban De Luca; Thierry Chevallier (BIODEVICES, 2023)

Shaping User-Centered Health Innovation Through Assessment. - Arthur Trognon; David Servais; Islem Habibi; Robert Picard; Thomas Lihoreau; Lionel Pazart; Sylvia Pelayo; Thierry Chevallier; Kathryn Ernecq; Anaïs Garin; Mathias Béjean; Denis Abraham (BIODEVICES, 2023)

Use of a Digital Positioning and Categorisation Aid for Clinical Investigations on Medical Devices: Questioning the Complexity of the Field and Harmonizing Stakeholders' Understanding. - Jean-Baptiste Pretalli; Stéphanie Py; Fatimata Seydou Sall; Magali Nicolier; Karine Charrière; Thierry Chevallier; Thomas Lihoreau (BIOSTEC (1), 2024)