Webinar | Safer medical devices: Implementation of the EU MDR and EUDAMED database

The Road to Market Authorization for Sterile Medical Devices within the EUПодробнее

EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745Подробнее

Celegence EUMDR Webinar - How To Start Preparing Your RA QA Team For The EUDAMED DatabaseПодробнее

The EUDAMED database and EUDAMED loginsПодробнее

TGA Webinar: Unique Device Identification #1Подробнее

The New EU MDR PMS Requirements WebinarПодробнее

Current Challenges in MDR (Medical Device Regulation) in the EU - Webinar with NO-FEAR ProjectПодробнее

How and When to Register EU Medical Devices and Report UDI Information to EUDAMEDПодробнее

Webinar | Medical Devices Regulation – Heading in the right direction?Подробнее

Clinical Evaluations for Unique Product Types Under the EU MDR – WebinarПодробнее

UDI and the EU MDR What You Need to Know to ComplyПодробнее

Best Practices for UDI Implementation and EUDAMED Submissions – WebinarПодробнее

Medical Devices - An Introduction to the EU EUDAMED systemПодробнее

European Database for Medical Devices (EUDAMED) RegistrationПодробнее

How to make labelling regulatory compliant for EU-MDR (2017/745)Подробнее

Medical Devices Regulation TrainingПодробнее

Webinar // Cybersecurity in the medical devices – How to show compliance to regulatory requirementsПодробнее

Part 1: Exploring EUDAMED Requirements for EU MDRПодробнее

MDR and IVDR update: Overview and status of EU and national implementationПодробнее