Follow
With Solectrix's SXIVE Sensor Configuration Tool, embedded vision developers can configure sensor registers quickly and efficiently—regardless of manufacturer. An open-source approach that simplifies the development process and fosters innovation.
We're excited to share the successes of our customers & to be there to help you as you improve the way you bring safer, faster medical devices to market.
Securely connecting hospitals and laboratories is vital for better treatments and diagnoses. But how can we ensure data security? Discover how robust software solutions safeguard patient safety and ensure data privacy.
Essential for all projects, software testing ensures high-quality, reliable products. A professional process reflects commitment to quality, adhering to guidelines for functional, stable, secure systems.
While cybersecurity is an important topic in many fields, it's a major issue for Medtech and medical devices. It's essential to put a strategy in place from the very start of your development, and to commit to a real discipline of follow-through.
We provide an innovative tool to manage your IFU digitally and in full compliance with MDR/IVDR regulation for your medical device and in vitro diagnostic devices. This will result in huge savings and burden reduction for your company.
The requirements for the technical documentation of a medical device are becoming significantly more extensive and demanding as a result of the MDR. Is it still possible to map the complexity using Word and Excel, or is it necessary to access digital solutions using "content management"?
Imagine if you could quickly and easily replace the previous Excel checklists with a guided process from requirements definition to approval documentation. We show you how!
To maximize your chances of getting a CE mark in time, the Quality of the Technical Documentation will be of crucial importance. Aligned Elements can help you find and eliminate quality errors in your Technical Documentation with less effort and in less time - Karl Larsson explains how.
At St. Jude Medical (now Abbott), multiphysics simulation is used to model left ventricular assist devices (LVADs) to improve the outlook and quality of life for patients with heart failure.
Spending too much time on design documentation and traceability? We can help! Develop medical devices smarter and faster with Aligned Elements.
Zürich, Switzerland
Swiss Medtech Expo is the trade fair for Europe's third-largest medtech market. With a practical focus on novel designs, materials, technologies and processes, the spotlight is on how integration and development of new applications leads to innovations in the medtech industry.
Luzern, Switzerland
TS Quality & Engineering is a ISO 13485 certified company. We offer Medical Device Consulting Services and solutions aimed at facilitating, speeding up and support design, validation, regulatory and quality control process. We can follow the design and development of a new product at all stages.
Zug, Switzerland
COMSOL is a global provider of simulation software for product design, engineering, and research in technical enterprises, labs, and universities. The flagship product, COMSOL Multiphysics® is an integrated environment for creating physics-based models and simulation applications.
Debiotech is an ISO13485 certified company, active in the development of innovative medical devices, with over 30 years of experience and know-how.
Lausanne, Switzerland
As a system supplier, Solectrix GmbH develops and produces electronic assemblies, software and FPGA modules as well as complete systems for demanding applications in medical technology.
Fürth, Germany
avasis has been your competent partner for the implementation of software solutions for the product lifecycle for over 25 years. We are a leading provider of digitization services for small, medium and large companies with a focus on the medical technology and machinery industries.
Berneck, Switzerland
ERNI steht für Swiss Software Engineering und schafft Mehrwert für Kunden durch die Bereitstellung methodenbasierter Consulting Services, partnerorientierter Technologie-Services und kostenbewusster Delivery-Services auf einer globalen Plattform, die auf einem Schweizer Mindset beruht.
Matrix Requirements GmBH is a global software leader helping innovative Medical Device companies remain focused on developing safer products faster. MatrixALM & MatrixQMS reduce the regulatory burden by bridging the gap between agile & compliance to ensure quality across the entire product lifecycle
Kehl, Germany
