Class 3 Medical Device EU MDR

Understanding Regulation (EU) 2017/745, Article 117 for Combination DevicesПодробнее

How to Prepare a Medical Device 510k Submission for FDAПодробнее

10 Things You Must Know About Updating Your Technical Files to Comply with EU MDRПодробнее

EU MDR: How Do I Interpret The New Regulations and What Do I Need to Do to Be Compliant?Подробнее

Navigating the EU Medical Device Regulation 2017/745Подробнее

MDR Transition Timeline Extension – The Impact on ManufacturersПодробнее

Introduction to different classifications rules for medical device softwareПодробнее

Medical Device News february 2024 Regulatory UpdateПодробнее

Medical Device News April 2024 Regulatory UpdateПодробнее

Classification of Medical Devices - EU 2017/745Подробнее

Webinar: Comparison Between the SFDA's New Regulations and the EU MDR #WebinarWednesdayПодробнее

Vigilance MD PSURs for Medical DeviceПодробнее

Is the EU MDR Extension a Blessing or a Curse? - WebinarПодробнее

What are Common Specifications Under EU MDR and IVDR?Подробнее

From MDR to NMPA (Chinese registration) of medical deviceПодробнее

EU Postmarket Surveillance Requirements for Medical DevicesПодробнее

Webinar: EU Medical Device Regulations and their impact in Australia | AHK AustralienПодробнее

Transitioning from MDD to MDRПодробнее

Medical Device RegulationПодробнее

Is my Software a Class I Medical device? [EU MDR 2017/745]Подробнее