MedtecLIVE

Check technical documentation for MDR compliance using Nakamo’s regulatory AI

Inconsistencies, gaps and a lack of traceability in technical documentation sometimes only come to light when the notified body identifies them. Nakamo’s AI companion “Flurina” systematically checks your documentation before it becomes a problem.

BAYOOSOFT GmbH

May 3, 2024

Best practice

Saving time when creating technical documentation — opportunities with a digital solution

Digitalization is constantly changing the way we work. Efficient digital tools and automation are key to minimizing workloads and gaps in technical documentation.

MedtecLIVE 2024

BAYOOSOFT GmbH

May 4, 2026

Product

Digital efficiency in quality management: Break free from the hamster wheel of documentation – with eQMS

Between increasing regulatory demands and growing complexity, manual QMS processes reach their limits. A digital eQMS reduces effort, increases transparency, and enables structured, audit-ready processes.

JÜKE Systemtechnik GmbH

February 19, 2024

Innovative Product Development and System Integration

Our experts translate customer requirements into reliable technical solutions, program firmware and software and provide standard-compliant documentation in accordance with the required norms and standards.

MedtecLIVE 2024

Zeller + Gmelin GmbH & Co. KG

January 20, 2026

MedTec Care Plus – our holistic concept for medical technology

From lubricant selection and service analyses to digital documentation – with MedTec Care Plus, we offer more than just an oil. With MedTec Care Plus, Zeller+Gmelin offers a holistic approach that goes far beyond mere lubricant development.

mecora Medizintechnik GmbH

April 30, 2026

Precision in a Controlled Environment

We specialize in the production of complex, customized plastic products for medical technology. We support you from development through to sterile-packaged products, including standard-compliant documentation.

Früh Verpackungstechnik AG

March 24, 2026

Sterilization as the interface between product, process and evidence

For many medical devices and packaging systems, sterilization is a critical interface between product design, process definition and regulatory evidence. This is where microbiological data, validation strategy and documentation requirements must be considered together.

XENON Automatisierungstechnik GmbH

April 18, 2026

Product

Automated Assembly and Testing of Drug Delivery Devices: Precision in Medical Technology

Learn more about high-precision automation solutions for drug delivery devices. From small series to high-performance lines, our concepts ensure cleanroom compatibility, seamless documentation, and the safe handling of the smallest components.

Metecon GmbH

February 17, 2025

Innovation Expo

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.

Providers related to 'Documentation' (49)

Genthner GmbH SystemTechnologie

Schnell, zuverlässig und vieles mehr. Seit über 35 Jahren deckt GENTHNER SystemTechnologie wichtige Bereiche der Produktion von Partnern aus der Medizintechnik, Luft- und Raumfahrt sowie der Feinmechanik und Messtechnik ab.

Birkenfeld, Germany

TEBIT Medical Devices GmbH

TEBIT is your partner when it comes to realizing medical technology ideas. As an ISO 13485-certified manufacturer, we support you in production and documentation with our solutions.

Meinerzhagen, Germany

Qosina

Qosina is a global supplier of 5,000+ single-use components for medical and pharma manufacturers. With 45+ years of expertise, we help engineers accelerate development through free samples, CAD files, low MOQs and reliable supply—supporting projects from concept to production.

Ronkonkoma, United States

velixX GmbH

Perfect Healthcare Solutions! Consulting and product development for Healthcare Products We provide you with solutions - the more complex, the better for us! MedTec - IVD - Analytik - Microfluidic - Micromechanics - That's our world

Mannheim, Germany

COSMO CONSULT SE

COSMO CONSULT supports medtech companies with Microsoft-based ERP, CRM, analytics, cloud and AI solutions. Specifically, we specialise in digitalised manufacturing, offering automated testing, intelligent decision-making and analysis to ensure efficient, transparent and secure processes.

Berlin, Germany

BYTEC Medizintechnik GmbH

For over 30 years, BYTEC Medizintechnik has been a service provider for the development and production of medical devices for surgery, therapy and diagnostics.

Eschweiler, Germany

KunststoffXtra - Das Magazin für Werkstoffe, Verarbeitung und Anwendung

The trade journal KunststoffXtra provides specialist knowledge—from practice, for practice. KunststoffXtra is the official publication of kunststoff.swiss. The magazine is published seven times a year and provides expert information on technical developments and industry trends in the plastics indus

5610 Wohlen, Switzerland

Metecon GmbH

Metecon GmbH - your regulatory compliance partner. For more than 25 years we have been supporting manufacturers of medical devices and IVDs with reliable solutions in QMS, Clinical Affairs, Regulatory Affairs and PMS. Tackle regulatory challenges efficiently with Metecon - let's get in touch!

Mannheim, Germany

QT9 Software Ltd

QT9 QMS is a fully integrated electronic quality management system (QMS) that unifies processes, documentation and compliance in one platform. With 25+ modules, real-time metrics and pre-validated workflows, it helps organizations streamline operations, ensure compliance and scale securely.

Killarney, Ireland

Jun 26, 2025 3:00 PM - 3:15 PM | automatica Summit Stage (B4.331)

Events related to 'Documentation' (2)

Exhibitor Presentation

Regulatory Compliance meets Manufacturing Excellence - MES enabling MDR compliant manufacturing

Exhibitor Presentation

May 7, 2026 11:30 AM - 11:50 AM | Exhibitor Forum (3-347)