Guide for start-ups – Regulatory Affairs & Design Assurance essentials
Start-ups that want to bring a medical device to market are inevitably confronted with a plethora of questions regarding compliant…
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Cybersecurity for medical devices
Medical devices are often connected to networks and can be vulnerable to cyber-attacks, which can compromise patient safety and the…
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Consultant Spotlight – Daniel Flury
Daniel Flury joined us in August last year as a Senior Consultant in the Quality team. In his Consultant Spotlight,…
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MedTech news roundup May 2023
Our May 2023 MedTech news roundup includes Swiss Medtech’s position paper on medical device procurement for the Swiss population, Swissmedic’s…
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MedTech news roundup April 2023
Our April 2023 MedTech news roundup covers the latest on the EU MDR & IVDR amendment, guidance news from Switzerland…
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How will the EU Green Deal impact the medical device industry?
The European Green Deal is a set of policy initiatives on climate action laid out by the EU Commission that…
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How to choose the right QMS
Whether you’re part of a large, well-established company with an existing Quality Management System, or involved in a start-up that’s…
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MedTech news roundup March 2023
Our March 2023 MedTech news roundup includes the latest on the EU MDR extension, Swiss Medtech’s Annual Report, and the…
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