Join Us at Our ‘Medical Device Product Life Cycle’ Conference: Putting Patients First with Henrik Eriksson
At Key2Compliance, we believe in the power of impactful storytelling! We’re thrilled to announce Henrik Eriksson, a dialysis patient with years of firsthand experience, as our esteemed opening speaker at our “Medical Device Product Life Cycle” Conference in October. Henrik Eriksson’s insights offer a unique perspective, setting the stage for a conference filled with inspiration […]
Webinar – Elevate your Career: Insights on progression within MedTech Quality Assurance
Join us for a live webinar exploring the many opportunities within Quality Assurance for MedTech Professionals, hosted by industry experts from Key2Compliance Whether you are just starting out or looking for mid-career progression, this webinar will equip you with practical strategies and actionable steps to support a successful career in MedTech Quality Assurance. You’ll have […]
Four Notified Bodies Headline the Medical Device Product Life Cycle Conference 2024
Mark your calendars for October 8 and 9th, because Key2Compliance is bringing back the fantastic conference, “Medical Device Product Life Cycle”, to Stockholm! This time we’re excited to let you know that we’ve got an exceptional lineup of speakers from four Notified Bodies: Sharmila Gardner, Technical Documentation Manager & Head of UK Approved Body, from Intertek […]
Join our breakfast event tailored to address the different approaches and best practices in supplier control
Are you seeking to learn more about how to ensure effective supplier control and outsourcing of processes, and which control strategies you can apply? Join us for an exclusive breakfast session tailored to address the different approaches and best practices in supplier control! Our experts Åsa Möllby, Director of Medical Device QA, and Oscar He, Product manager and Senior Consultant, […]
Clinical Insights Breakfast at Medicon Village: Navigating MedTech Challenges with Jeanette Demorney & Maria Lindgren
Are you looking to gain a better understanding of how to prepare for clinical investigations? After a successful event at Symbion in Copenhagen, we are now offering this unique opportunity in Sweden as well! We’ve put together this unique breakfast tailored to the challenges of clinical investigations in the MedTech sector. Join our experts Maria Lindgren and Jeanette […]
Regulatory Insights Breakfast: Navigating Lægemiddelstyrelsen’s Supplier Management Expectations in 2024
Did you know that Lægemiddelstyrelsen will prioritize Supplier Management in their inspections in 2024? Join us at Symbion in Copenhagen on the 15th of May. We’ve put together this unique breakfast to give you a quick introduction to what their expectations will be from a regulatory point of view and what questions you should be […]
Conference: Medical Device Product Life Cycle
Join us in boosting MedTech knowledge together! On October 8 and 9th, 2024, Key2Compliance is delighted to once again host the highly appreciated Conference, “Medical Device Product Life Cycle”, this time in Stockholm! We’re honored to have four Notified Bodies joining us as featured speakers at our event: BSI, RISE, Intertek, and TÜV SÜD. Featuring […]
Aligning clinical evidence and market access for you medical device
Join us on the 21st of March in Lund, when Key2Compliance will host the Medtech Network, organized by Medicon Valley Allicance. The manufacturer´s focus during the medical device life-cycle is to continuously ensure safety and performance of the device, this is done by iterating/updating the technical documents such as the clinical evaluation and risk management […]
Join our unique Breakfast Event!
🔬 Are you looking to gain a better understanding of how to prepare for clinical investigations? We’ve put together this unique breakfast tailored to the challenges of clinical investigations in the MedTech sector. Join our experts Maria Lindgren and Jeanette Demorney as they explore and discuss essential topics related to this specialized field. This event provides you with a […]
Medical Device Product Life Cycle – Boosting medtech knowledge together!
SAVE THE DATE Join our Medical Device Quality Assurance and Regulatory Affairs conference on the 8-9th of October in Stockholm, Sweden. This is an international conference focused on navigating the world of medical device regulations and standards. Our speakers will share their knowledge and tools to help you make complex things easier! We will outline […]