Join us for the latest Medical Device events, webinars and tradeshows with Matrix Requirements

Join us to understand how different regions categorize medical devices. Ensure compliance and remain empowered with the knowledge to navigate international regulatory landscapes confidently. 

How to Classify your Medical Device?

How to Classify your Medical Devices?

How to classify your Medical Device?

Do you want to implement AI in your medical devices, but unsure about regulations, methodologies and more?

Discover the full potential of AI as you develop your medical device.

Discover the full potential of AI as you develop your medical device

Developing AI-Powered Medical Devices

Excel in Software Testing and become experts in IEC 62304

Must know strategies for Medical Device Companies to Achieve Regulatory Excellence.

What qualifies as high-risk AI under the AI Act.  The AI Act’s Regulatory Framework with insights into compliance requirements and reporting obligations.  Discover effective strategies for conducting risk assessments on AI technologies in medical devices.   How to future-proof your Regulatory Approach to stay ahead of the curve.

High Risk AI under the European AI Act:

High Risk AI under the European AI Act

Webinar: High Risk AI under the European AI Act

Explore the latest insights in regulatory affairs through our webinar series. Stay informed and up-to-date on key industry topics

Webinar Navigating Regulatory Affairs

Launch Medical Device to Market in the EU vs US

Webinar: Launch Medical Device to market in US and EU

Essential strategies to empower your R&D teams through Agile!...

Agile Medical Device Development

Remain Agile with your Medical Device Development

Webinar: Agile Medical Device Development

Innovation for Health

We're so excited to attend this event, see you in Würzburg!

Regulatory Affairs Expert Talks

We look forward to meeting you in Dana Point!

LSI 

Let's meet at the 2024 edition of MedTech Meetup! 

MedTech Meetup 2024

MedInTechs

Essential Strategies for Effective Risk and Document Management.

Mastering EU MDR

Webinar: Mastering EU MDR

During this webinar, we will talk about what is important to build a regulatory strategy in the different phases of a company.

Webinar: Navigating Regulatory Affairs in your Medtech Startup

Join this webinar to gain a better understanding on how your R&D, QA and Compliance teams can work better together. 

Webinar Bridging The Gap Agile/Compliance

Webinar: Bridging the gap between Agile and Compliance

Come and meet the team at the booth B2062 at Swiss Medtech Expo 2023!

Swiss Medtech Expo

LSX Boston 2023

LSI Europe '23

Looking forward to meet you at BioMedevice Boston 2023!

BioMedevice Boston

Medical Technology Ireland

Looking forward to see you at the MEDICEN DAY 2023!

Events