This forum is a collection of stories and content from our team that talks about what’s happening in the medical device industry, the changing landscape, and how companies and talents are positioning themselves.
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Thomas Meininghaus, Vice President of Regulatory Affairs at Ottobock, shared with us how having a background in general management and operations can change and help your perception as a regulatory affairs professional.
In this blog, guest blogger, Katarzyna Wesołowska, Chief Executive Officer at MDR Regulator, explained How to build an effective MDR strategy for cooperation with Importers, Distributors and Authorised representatives?
In this new episode of our ‘A day in the life of’ mini-series, we spoke to Lea Atallah, Quality and regulatory affairs manager at Zimmer Biomet.
In this blog, guest blogger Elly Gysels, Head Regulatory Affairs at Sensile Medical, explains product documentation: why you care about it and how to improve it.
Maria Fagan & Lisa Casavant, Co-founders of RQM+, formerly known as R&Q takes us through the story behind the market leading consultancy RQM+.
A message from our Founder Elena Kyria CEO Elemed As a fully female recruitment company active in the medtech industry, our role in advancing the
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