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.
Why do MedTech and medical device startups need ISO 13485 certified quality management systems? Now is an extremely exciting time to be a medical device
5 signs of a great regulatory affairs recruitment agency Finding regulatory affairs talent – especially at a senior or leadership level – can be a
In this special episode, we spoke to Kimberly Trautmam, Medical Device, IVD, and Combination Product Regulatory & Quality Expert, about being fearless: seize the opportunities that scare you the most.
What is post market surveillance for medical devices? Your new, cutting-edge medical device has been designed and tested, and is ready to get out into
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What is Elemed’s expert corner?
It is a hand-selected group of individuals that have been identified as top
voices/thought leaders in their space.
Why should you take part?
This is a great opportunity for you to raise your personal brand awareness, your company’s reach in the market, but also to provoke wider discussion. It will establish yourself as an authority in the space and enhance your professional image.
Get in touch with Mathilde at [email protected] to find out more and/or take part.
Let’s get to know each other
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