In our online library, you will find a collection of links to useful resources on the European medical devices legislation and associated topics, like guidance and legislation documents, factsheets, list of notified bodies, European authorities websites etc.
Links to our five main library sections
Please use the following links to enter each topic with a wide range of documents, websites, information and hints.
- Download Section Legislation Documents
- Download Section Guidance Documents MDR
- Download Section Guidance Documents IVDR
- Supportive Information for Manufacturers of Medical Devices and In Vitro Diagnostics
- Complete Link Section for Manufacturers of Medical Devices and In Vitro Diagnostics
Although mdi Europa is constantly reviewing this sections, please be aware that we listed only the most important documents and links. Should you require a specific information that is not listed, please get in touch with us.
To reach out for even more information, browse all articles on the mdi Europa website by keywords
Artificial Intelligence (4) BfArM (6) Brexit (20) Certificates of Free Sale (2) Checklists (3) Clinical Evaluation (12) COVID-19 (17) EU Authorized Representative (5) EUDAMED (18) European Commission (50) Featured Content (3) Guidance Documents (79) IVDD (4) IVDR (123) Legacy Devices (26) Legislation Documents (20) MDCG (49) MDD (3) MDR (143) Medical Devices (6) News in Brief (40) No-Deal Brexit (9) Notified Body (25) Performance Evaluation (6) Security Advice (5) Templates (3) UDI (8) Unique Device Identification (5) Vigilance (7) WHO (3)