Medical Device Newsletter
Dear Reader,
In this month’s issue, we share highlights from our recent Medical Device Software webinar series, now available on-demand for those developing software that impacts patient health.
If you're involved in clinical investigations our latest white paper 'Clinical Investigations Under MDR' offers a deep dive into the MDR requirements. Explore key aspects such as obtaining authorization, the responsibilities of the EU Legal Representative, and the MDR’s influence on study conduct and post-market surveillance
Looking to connect? Join us this November at MEDICA in Düsseldorf, where industry experts from around the world gather. And, as always, stay updated with key regulatory changes, including the latest MDCG guidance and newly published harmonized standards.
Happy reading!
Paolo Guerra - Business Development Director MedTech
Medical Device Software: The Journey from Idea to Patient for Successful Market Access
Our recent webinar series, delved into the Medical Device Software Life Cycle, covering critical topics like software validation, regulatory compliance, and clinical evidence. Through each session, we highlighted best practices and industry standards that medical device companies need to achieve innovation and regulatory success.
Didn’t have the chance to join live? You still have the opportunity to access these insights anytime and watch the webinars on-demand.
Are you looking for expert guidance in your medical device software journey? Whether you’re working on new software development or optimizing existing systems, we’re here to support you.
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SEE YOU THERE?
?? 11-14 Nov | ??Düsseldorf, DE
In November, MEDICA will once again bring together international experts from the medical industry in Düsseldorf, Germany. We will also be there! If you have any questions about medical devices, visit our booth at Hall 4, E48. Want to know more about our IVD services? Let's have a chat at booth G92, Hall 3.
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