Видео с ютуба Technology For Ivdr Compliance

CAPTIS™ - Technology for EU MDR & IVDR Compliance

CAPTIS™ - Technology for EU MDR & IVDR Compliance

A Roadmap for MDR and IVDR Compliance With QMS

How to create your Medical Device Technical File [EU MDR & IVDR]

Which devices can be sold as Legacy Devices under IVDR after May 26, 2022?

Краткий курс по Регламенту ЕС 2017/745 о медицинских изделиях

In Vitro Diagnostic Regulation - IVDR

Understanding the MDR & IVDR: What Medical Device Companies Need to Know.

Smart technology enables a holistic, data-driven approach to EU MDR/IVDR

Preparation for the In Vitro Diagnostic Regulation IVDR 2017/746

Your Partner for MDR and IVDR Compliance

ESHG IVDR Webinar: Section 3 - IVDR - Obtain regulatory compliance for IH-IVD’s

IVDR compliance: tips and best practice

Easy Reference Management with CAPTIS™ - Software for EU MDR and IVDR Compliance

EUDAMED Webinar | MDR & IVDR Compliance Explained

IVDR tutorial for diagnostic labs 7: Guidance, concerns, recommendations

MDR Technical Documentation Requirements | MDR and IVDR Compliance Webinar

Looking to master In Vitro Diagnostic Medical Devices Regulation (IVDR)?

IVDR Guidance

In vitro diagnostic medical devices & Regulations IVDR consultancy - MDR Regulator