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 […]
Meet us at E-Sundhedsobservatoriet 11-12 October
Attention Software developers! Is you software a medical device? Are you prepared for MDR? Key2Compliance specialize in guiding software companies through the complex process of CE certification. Join us at our stand at E-Sundhedsobservatoriet on the 11-12th of October and talk to our experts Susanne Søeborg and Cecilie Bengtsen. Whether you need assistance with the entire certification project […]
Meet us at Medicinteknikdagarna October 9-11th
Come and meet us at Medicinteknikdagarna on October 9-11th! Visit our stand and have a chat with our experts Tomas Camnell and Helena Dahlin and learn more about Key2Compliance and how we make complex things easier for Medical Device and IVD companies. We hope to see you there! 📅 October 9-11th 📍BioClinum, Karolinska Sjukhuset, Stockholm
Sign-up to our upcoming FREE breakfast club WEBINAR!
Rise and shine Medical Device Software manufacturers! Get your coffee ready and sign-up for to our upcoming FREE breakfast club WEBINAR on October 19th, at 09.00! Join a 30-minute discussion with our experts about the MDR Transition period – What impact will it have on Medical Device Software (MDSW)? In the beginning of 2023, EU […]
Free webinar: Monitoring and electronic master file
See the recording here >> Join our latest webinar on the 1st of June where our first speaker, Susanna Hellström, Consultant Clinical Development will present the role of the monitor in clinical studies. You will get a brief overview of the visits they perform and obstacles they can encounter working with a study. Kristina Edner, […]
Join our international 2-day conference in Copenhagen on the 4-5th of October!
This is a must-attend conference for all medical device professionals dealing with biological and/or clinical evaluations, Clinical operations, QA/RA Managers, R&D managers and CEO:s. This conference will address biological and clinical evaluations from a risk perspective through a mixture of presentations from standard developers, notified bodies, test houses and device manufacturers. The first day will […]
Welcome to join Innokas Medical and Key2Compliance´s Good Morning Meeting at Medicon Valley!
Optimal Regulatory and Design Development from Idea to Success of a Medical Device To succeed in taking a medical device product from idea to the market, both the design and development flow, as well as the regulatory flow need to be considered. As the inventor or manufacturer of a medical device, a key success factor […]