Consulting and Services

The ABCs of Product Lifecycle Reporting under the MDR – How to Stay on Track!

The requirements of the MDR for the documentation of medical devices are complex. However, with the right strategy, it’s not rocket science to efficiently implement all phases – from clinical evaluation to post-market surveillance.

BIOCOM Interrelations GmbH, medtech zwo

February 14, 2025

Novelty

Newly published: 10th Guide to German Medtech Companies 2025

The anniversary edition of the Guide to German Medtech Companies has just been published in cooperation with the Medtech-zwo partners Medical Mountains, SPECTARIS, IVAM, bayern innovativ Gesundheit, Medical Valley EMN, microTEC Südwest e.V., GTAI German Trade & Invest and VDMA.

softgate GmbH

February 5, 2025

🏥 Medical technology innovation – developed locally, impacting globally 🌍

At softgate, we combine technical expertise, regulatory know-how, and regional proximity to create tailored solutions that drive innovation in healthcare.

softgate GmbH

February 5, 2025

😴Dreams do come true!

….. Or weren’t you dreaming of SDC and the endless possibilities of device communication and interaction? 🚀 Seamless medical device communication with SDC

TÜV Rheinland AG

January 29, 2025

Chemical safety of medical devices is essential. Topics such as biocompatibility in accordance with DIN EN ISO 10993-18

Chemical safety of medical devices is essential. Topics such as biocompatibility in accordance with DIN EN ISO 10993-18 and the regulation of PFAS are in the spotlight. Find out how to minimise risks and efficiently implement regulatory requirements.

Metecon GmbH

January 27, 2025

The Perfect Combination: RIM System and Regulatory Services

Implementing a RIM system? Even the best software isn’t enough on its own. Rely on the perfect combination of a technological system and human expertise.

TÜV Rheinland AG

January 27, 2025

How can we trust artificial intelligence? On the opportunities and risks for the medical technology industry.

The medical technology industry is currently undergoing a transformation through the integration of artificial intelligence into the software of medical devices. This innovation opens up countless opportunities for improvement. Dr. Andreas Schwab/TÜV Rheinland sheds light on developments/challenges.

be-on-quality GmbH

January 24, 2025

You Develop Medical Devices - We Handle The Rest

Our business areas - expertise for the success of your medical devices In a constantly changing and highly regulated industry, our team of experts offers customized solutions to bring your medical devices to market safely and efficiently. Our services include:

Past events (9)

Jun 20, 2024 11:30 AM - 12:00 PM | Exhibitor Forum (1-916)

Simplify your post-market surveillance work with the help of AI

MedtecLIVE 2024

Jun 19, 2024 4:00 PM - 4:30 PM | Exhibitor Forum (1-916)

The Digitalizers: From movie cameras to rear-view mirrors and microscopes – how Solectrix leads sector after sector out

MedtecLIVE 2024

Jun 19, 2024 3:00 PM - 3:30 PM | Exhibitor Forum (1-916)

Digitalization - the basis for compliance with regulations and the basis for the use of AI in medical technology

MedtecLIVE 2024

Jun 19, 2024 1:30 PM - 2:00 PM | Exhibitor Forum (1-916)

Everyone is talking about digitalization - we are doing it, learnings and best practices from customer projects

MedtecLIVE 2024

Jun 19, 2024 1:00 PM - 1:30 PM | Exhibitor Forum (1-916)

Unfortunately canceled! Deus Ex Machina - Digitalisation will solve all of your problems

MedtecLIVE 2024

Jun 19, 2024 12:00 PM - 12:30 PM | Exhibitor Forum (1-916)