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Regulation

Whether it's the European Medical Device Directive (MDD) or other international regulations. It is important for the medical device industry to keep abreast of the latest regulatory developments.

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Andrey Kostychev
Caroline Schmidt-Lucke
Paolo Guerra
Iryna Ruda
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Posts - that's to be discovered on the topic (40)

Logo FOBA Laser Marking + Engraving | ALLTEC Angewandte Laserlicht Technologie GmbH

FOBA Laser Marking + Engraving | ALLTEC Angewandte Laserlicht Technologie GmbH

June 29, 2026

Compliant Labeling of Active Implantable Medical Devices: When Precision and Quality Ensure Life

Active implantable medical devices (AIMDs), such as pacemakers or neurostimulatory systems, perform vital functions in the human body. Accordingly, the requirements for quality, safety, and reliability are high—including in labeling, which is central to unique identification and traceability.
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BAYOOSOFT GmbH

May 4, 2026

Medical technology regulation reimagined: Structure instead of complexity with DIN SPEC 91509

How a standardized data model is reshaping medical technology regulation and enabling more efficient, transparent, and scalable compliance processes today.

MedtecLIVE 2026
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Solectrix GmbH

April 28, 2026

Your partner throughout the entire development cycle

We support you at every stage and ensure that regulatory, standard-related and quality aspects are an integral part of your project right from the start.

MedtecLIVE 2026
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Metecon GmbH

April 27, 2026

Regulatory Resilience: Why MedTech Companies Need a New Approach

Many organisations meet regulatory requirements yet operate on systems that react poorly to change. This article explains why resilience is becoming a core capability for MedTech – and how companies can build it step by step.

MedtecLIVE 2026
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NewTec GmbH

April 22, 2026

Secure Development of Medical Technology: Safety, Security & MDR Compliance

Learn how to master the challenges of the MDR and efficiently develop safety-critical medical technology. From safety and security to usability engineering.

MedtecLIVE 2026
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QT9 Software Ltd

April 21, 2026

EUDAMED 2026: Is MedTech Ready for Full MDR Enforcement?

EUDAMED is rapidly evolving into an active regulatory environment that exposes gaps in compliance readiness. Learn how a connected eQMS like QT9 helps unify all requirements consistently and safely meet MDR mandates for 2026.

MedtecLIVE 2026
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Ingenics AG

April 18, 2026

Balancing Innovation and Regulation in the Medical Device Industry Cost-Effectively

In medical technology, balancing innovation with strict regulation is critical. Learn how to reduce costs through optimized processes and strategic consulting while ensuring full compliance for your medical devices.

MedtecLIVE 2026
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GBA Group MedTech Solutions

April 16, 2026

Welcome to GBA Group MedTech Solutions

Your trusted partner for analytical services, validation, and compliance. We support you in bringing your medical devices to market safely and efficiently while meeting regulatory requirements worldwide.

MedtecLIVE 2026
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Lorit Consultancy

April 15, 2026

Master Medical Device Compliance: IEC 60601, IEC 62304 & Cybersecurity

Struggling with safety standards, software processes or cybersecurity requirements? Get clear, practical guidance to finally move your product towards approval.

MedtecLIVE 2026
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QT9 Software Ltd

April 9, 2026

Automate Quality and Compliance with QT9 QMS

See why more than 1,200 users trust QT9's full-suite QMS software to automate audits, streamline operations and scale safely. Get accessible control and regulatory excellence.

MedtecLIVE 2026

Past events (4)

May 6, 2026 3:30 PM - 4:30 PM | Forum (3-520)
MedtecLIVE 2026

Adequate information security for medical devices

MedtecLIVE 2026

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Logo ZVEI e.V.
D
May 6, 2026 2:00 PM - 3:00 PM
MedtecLIVE 2026

Win a Free Ticket for the Usability & Human Factors MeetUp

MedtecLIVE 2026

Logo USE-Ing. GmbH
D
May 5, 2026 3:30 PM - 4:45 PM | Forum (3-520)
MedtecLIVE 2026

The Future of SMEs in Germany’s Medical Technology Sector: Hope Through MDR Reform?

MedtecLIVE 2026

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Logo BVMed - Bundesverband Medizintechnologie e.V.
Christopher Kipp
Jan Birkholz
Paul Malinovski
Dr. Annette von der Groeben
Christina Urschidil
May 5, 2026 12:30 PM - 12:50 PM | Exhibitor Forum (3-347)
MedtecLIVE 2026

Wonderful World of Biocompatibility. Recent Updates and Challenges

MedtecLIVE 2026

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Logo Eurofins Medical Device Services
Kristin Rödig

Providers (22)

Früh Verpackungstechnik AG

We offer comprehensive services from a single source - in the highest quality, for the best possible protection of products, people and customers. From the development of customized solutions to the production of packaging materials and contract packaging to qualification and documentation.

Fehraltorf, Switzerland

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Logo JÜKE Systemtechnik GmbH

JÜKE Systemtechnik GmbH

JÜKE is an experienced service provider for product development, contract manufacturing and regulatory affairs for companies in the fields of medical technology, analytics, biotechnology, laboratory technology and photonics.

Altenberge, Germany

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FOBA Laser Marking + Engraving | ALLTEC Angewandte Laserlicht Technologie GmbH

FOBA Laser Marking + Engraving (brand of ALLTEC Angewandte Laserlicht Technologie GmbH) develops and supplies advanced laser technology for industrial direct part marking and engraving.

Selmsdorf, Germany

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MedtecLIVE

MedtecLIVE is the leading trade fair in Europe for the development and manufacture of medical technology

Nürnberg, Germany

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Logo MedicalMountains GmbH

MedicalMountains GmbH

MedicalMountains GmbH is a network that connects and supports players in the medical technology sector. We promote the exchange between companies, research and politics and create platforms for dialogue. We support all players in the medical technology sector.

Tuttlingen, Germany

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Logo Hohenstein Laboratories GmbH & Co. KG

Hohenstein Laboratories GmbH & Co. KG

Hohenstein is your partner for testing & evaluation of medical devices

Bönnigheim, Germany

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Logo BAYOOSOFT GmbH

BAYOOSOFT GmbH

Focus on the essentials and increase productivity. Simplify, delegate & automate your management processes in highly regulated areas and critical infrastructures.

Darmstadt, Germany

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Logo novineon CRO GmbH

novineon CRO GmbH

novineon CRO is a leading service provider for research and regulatory affairs. For two decades we have been supporting manufacturers of medical devices and in-vitro diagnostics (IVD) in clinical and regulatory affairs related to conformity issues, e.g. clinical evaluation and clinical trials.

Tübingen, Germany

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Logo NMI Naturwissenschaftliches und Medizinisches Institut

NMI Naturwissenschaftliches und Medizinisches Institut

With pioneering innovations at the interface of medicine, natural sciences and engineering. Our mission is the transfer of knowledge and technology into practice. Our guideline: NMI achieving results!

Reutlingen, Germany

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