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Shaping User-Centered Health Innovation Through Assessment., , , , , , , , , and 2 other author(s). BIODEVICES, page 229-242. SCITEPRESS, (2023)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)., and . BIODEVICES, page 273-280. SCITEPRESS, (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., , and . BIODEVICES, page 215-221. SCITEPRESS, (2023)The Role of Massive Databases in the Post-market Clinical Follow-up of Medical Devices., and . BIODEVICES, page 243-249. SCITEPRESS, (2022)Threats and Opportunities for the Clinical Investigation of High-risk Medical Devices in the Context of the New European Regulations., , , , , , , , , and 5 other author(s). BIODEVICES, page 274-284. SCITEPRESS, (2021)Use of a Digital Positioning and Categorisation Aid for Clinical Investigations on Medical Devices: Questioning the Complexity of the Field and Harmonizing Stakeholders' Understanding., , , , , , and . BIOSTEC (1), page 864-871. SCITEPRESS, (2024)Combined Medical Devices: Which Classification for These Borderline Products and Which Consequences for the Manufacturers - About a Use Case in Skin Healing Area., and . BIODEVICES, page 281-288. SCITEPRESS, (2022)Contribution of Methodologies Adapted to Clinical Trials Focusing on High Risk Medical Devices., , and . BIODEVICES, page 337-343. SCITEPRESS, (2020)