EXCO - Your Trusted Partner for ISO-Certified Quality
Discover our project references and learn how we support our customers in GxP-regulated environments with proven, practical solutions.
eCRF development and implementation for clinical data management
EXCO designs, specifies, develops, and implements eCRFs based on study protocols, enabling clinical trial data to be collected in accordance with high quality standards.
Cybersecurity checklist for hearing aid software
EXCO developed a checklist for conducting a comprehensive risk assessment after several audit deviations in the area of cybersecurity were identified at the customer's site.
Medical device approval (FDA) with a focus on cybersecurity
EXCO provided cybersecurity support to the client in connection with FDA approval of an operating-theatre medical device under the eSTAR programme.
Risk Management and Product Approval
EXCO prepares companies for product audits and evaluates risk management files.
Design verification for a point-of-care device
EXCO provides support in the verification process of a glucose measuring device.
Accompaniment of MDR Product Licensing
EXCO advises a medical device manufacturer on the new European Medical Device Regulation (MDR).
