Time is running out – Join our conference!
We are beginning our countdown until our Medical Device Product Life Cycle Conference on October 26-27th! We are thrilled to see how many of you have signed up to join us. There are still some spaces left. If you haven’t yet registered, but are thinking about doing so, we encourage you to REGISTER NOW to […]
Meet Christoffer Ekström at the Medical Device Product Life Cycle conference
We are thrilled to announce that Christoffer Ekström, CEO at AI Medical Technology will one of the speakers at our conference “Medical Device Product Life Cycle” in October. 𝐅𝐫𝐨𝐦 𝐮𝐬𝐞𝐫 𝐧𝐞𝐞𝐝 𝐭𝐨 𝐩𝐫𝐨𝐝𝐮𝐜𝐭 𝐬𝐩𝐞𝐜𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧 – 𝐚 𝐫𝐞𝐚𝐥 𝐰𝐨𝐫𝐥𝐝 𝐞𝐱𝐚𝐦𝐩𝐥𝐞 Christoffer will share his story on how AI Medical Technology matched a critical user need with innovative technology and […]
Welcome to the team!
Welcome our newest rockstars to Key2Compliance, Heléne Lindegren, Malin Borg, Dalia Rhman och David Dahi. Four individuals who are joining us and no doubt will have a huge impact on their clients and teams! Welcome to the team! HELÉNE LINDEGREN, Business & Contract Manager What will be your role at Key2Compliance? My role at Key2Compliance […]
Meet our speakers at the Medical Device Product Life Cycle Conference!
We are excited and proud to have some of the most experienced speakers within the industry present at our Medical Device Product Life Cycle conference in Lund on the 26-27th of October. Become inspired, get the latest knowledge, and turn your compliance strategies into a tool for success! Meet our speakers: Erik Hansson, Senior Expert […]
Meet us at Nordic Life Sience Days!
Join us at the Nordic Life Science Days on the 28-29th of September in Malmö. This is the largest Nordic partnering conference dedicated to the life science industry. Stop by at booth 26 and meet our team- Jan Hellqvist, Tomas Camnell, Susanne Søeborg, Charlotta Hjerpe, Malin Löwenhoff and Terese Hedin. Learn more about Key2Compliance and how we make complex things easier for Medical Device, IVD […]
A warm welcome to our two new team members!
We are glad to share with you that our Key2Compliance team has recently been joined by two new team members – Erik and Susanna. We are excited to introduce you to these two talented additions to our team! ERIK BOM, Medical Device QA/RA Consultant What will be your role at Key2Compliance? I will work as […]
Key2Compliance establishes office in Denmark
Medtech and Pharmaceutical consultants Key2Compliance are now expanding outside Sweden’s borders for the first time. Recruitment has already started for the Danish office in Copenhagen. ”We already have a number of Danish customers and have completed numerous courses and training there. This was a natural step”, said CEO Jan Hellqvist. Key2Compliance has greatly expanded its […]
Free webinar: Is your medical device software MDR ready?
There are lots of great ideas and products related to medical device software today. Many of them already are compliant to the Medical Devices Directive (MDD), others are in an earlier development state. Since May 26th, 2021, the Medical Devices Regulation (MDR) is in force and latest May 26th, 2024, all medical device software has […]
FREE Webinar – An overview of IEC 62304 Medical Device software
Join us for this free webinar January 25, 2021 • 14.00-14.20 CET Learn more about how you can comply with the IEC 62304 standard in your Medical Device software development and maintenance process. When to apply IEC 62304? Overall development process for a medical device that is or includes Software Main points of IEC 62304 […]