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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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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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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Transferring your manufacturing site | What to consider regarding biocompatibility
Whether for economic or strategic reasons, medical device manufacturers often outsource their production to another site or external company. In…
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MedTech news roundup February 2023
Our February MedTech roundup covers news from Swiss Medtech regarding a pioneering data exchange platform, updates from the MDCG on…
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MedTech news roundup – January 2023
Our January 2023 MedTech news roundup covers the latest from Swissmedic regarding its strategic goals for 2023-2026 and advice on…
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MedTech news roundup – November 2022
Our November MedTech news roundup covers the recent Swiss-UK MRA, Swiss Parliament’s mandate to the Federal Council to adapt national…
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