Is My Software A Class I Medical Device

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

Easy Medical Device

Introduction to different classifications rules for medical device software

Medical Device HQ

Short course on the Medical Device Regulation (EU) 2017/745

Medical Device HQ

The ABCs of Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 - Webinar

Software as a Medical Device Classification Rule 11 (EU MDR 2017/745)

Easy Medical Device

Re-classification of software based medical devices

Using Selenium in the Verification and Validation Process for Medical Device Software | Lydia Tripp

Selenium Conference

What is Software as a Medical Device (SaMD) in Clinical Research?

GCP-Mindset - All About Clinical Research

Test Driven Development for Medical Devices

Bluefruit Software

Software Validation for Medical Devices – FAQs

Medical Device Academy

TGA Webinar: Regulation of Software As a Medical Device

Medical Device Software Development Short Course

Medical Device HQ

Embedded Software in Medical Device : Common Regulatory and Quality pitfalls

GMED North America

Short course on SaMD (Software as a medical device), IEC 62304 and IEC 82304-1

Medical Device HQ

Not So Fast: Is That Software Really Still A Medical Device?

Informa Markets - Engineering

ASTQB Webinar: How Software Testing is Different for Medical Device Software

ASTQB Communications

What is IEC 62304?

Medical Device Academy

Medical Devices Regulations Webinar - 24 January 2023

How is My Medical Device Classified?

U.S. Food and Drug Administration

Software as a Medical Device (SaMD): Clinical Evaluation- Demo