Clinical Investigation and Clinical Evaluation of Medical Devices

Short course on Clinical Investigation for Medical Devices and ISO 14155

Risk management for medical devices and ISO 14971 - Online introductory course

Как выполнить оценку эквивалентности продукта в отчете о клинической оценке (CER)?

How to perform the summative evaluation for medical devices (IEC 62366-1)

Short course on Usability Engineering for Medical Devices and IEC 62366-1

How to estimate risk for a medical device according to ISO 14971:2019

An introductory guide to medical device Clinical Evaluation & Clinical Evaluation Reports (CER)

Послепродажный надзор как требование к медицинским изделиям в ЕС

9 Tips to Improve Medical Device Design & Usability

Understanding Key Components of a Medical Device Clinical Evaluation

Medical Device Software Development Short Course

What is a medical device according to the MDR

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

The usability engineering process and key terms

Documentation for a medical device product development process (Part 1)

How to update your Clinical Evaluation Report (CER) for 2024

FDA 101 for Medical Devices

Artificial Intelligence in Medical Devices

UDI requirements for medical device manufacturers in the EU

Clinical Evaluation of Medical Devices prior and after MDR