We are your partner for the entire life cycle of medical devices – from development to post-market surveillance. We offer a comprehensive range of services with three independent services: consulting (including RA/QA), laboratory testing and sterile packaging for medical devices.
Eurofins Medical Device Services is your global partner for the entire life cycle of medical devices – from development to post-market surveillance.
Our comprehensive range of services covers three core areas:
Consulting (including regulatory affairs and quality assurance)
Our experts support manufacturers in meeting regulatory requirements, implementing quality management systems and preparing for audits.
From product approval to MDR and ISO compliance to post-market activities, we reliably guide you through all regulatory processes.
Laboratory testing
Our accredited laboratories perform testing in accordance with international standards, including biocompatibility, chemical characterisation, sterility and packaging validation tests to ensure the safety and compliance of your products.
Sterile packaging
We offer comprehensive solutions for sterile medical devices: cleaning, assembly, blister development, packaging, sterilisation, validation and complete documentation – all in accordance with ISO and MDR requirements.
