Is Your Innovation a Medical Device?
Demystifying Regulatory Pathways for Entrepreneurs Zahra MavajianRegulatory affairs and Quality assurance consultant – GBA Key2Compliance Are you an entrepreneur with great ideas to impact your field, whether through a new device, software, service, or system? If so, you might be wondering: Does my innovation fall under Medical Device Regulation? And more importantly, what happens if […]
IVDR Compliance Deadline – Are You Prepared?
The IVDR compliance deadline is here! If you’re a manufacturer, it’s crucial to ensure your Quality Management System (QMS) is compliant and your IVDR application is submitted to a Notified Body. For Class D IVD manufacturers, this includes submitting the application and getting a written agreement with a Notified Body by September 26, 2025. Ensuring […]
How ISO13485 prepares your IVDR Quality System for audits and what it doesn’t cover
Register today! May 27, 2025 10:30 – 11:15 CET Join our Free Webinar on IVDR Compliance for In Vitro Diagnostic Medical Device Manufacturers With the upcoming IVDR compliance deadline at the end of May, it’s crucial to ensure your organization is fully prepared. This webinar will provide a comprehensive overview of the most critical aspects […]
Navigating IVDR Certification: Prostatype’s Success Story with GBA Key2Compliance
Prostatype Genomics is at the forefront of precision medicine, offering the Prostatype® test—a groundbreaking genetic diagnostic tool designed to assess the aggressiveness of prostate cancer. By providing crucial insights, Prostatype helps clinicians and patients make informed treatment decisions, ultimately improving patient care and optimizing healthcare resources. Prostatype has an ability to significantly improve the quality […]
Simplifying IVDR Compliance: Insights from Senior Consultant Emily Malmberg
Emily Malmberg’s passion for medicine and biology led her from academia into the dynamic field of medical devices. As a Senior Consultant at GBA Key2Compliance, she leverages her extensive background to guide companies through the intricacies of the In Vitro Diagnostic Regulation (IVDR). “Transitioning from academia to the medical device industry allowed me to apply […]
The Important Role of a PRRC in Medical Device and Software Compliance
One of the changes introduced by the Medical Device Regulation (MDR) in 2017 and the In Vitro Diagnostic Device Regulation (IVDR), is the requirement of a designated Person Responsible for Regulatory Compliance (PRRC). A PRRC bears the important role mandated by the MDR and IVDR of maintaining the safety, integrity, quality, and effectiveness of medical devices. […]
Learn more about IVDR from the experts!
Key2Compliance has summarized some of the key challenges of the IVDR transition in a webinar. The webinar features expert consultants and industry professionals and helps companies understand the new regulations, and what its implementation means for them and their IVD devices. The speakers tackle various topics on the subject, ranging from key changes in the […]
Compliance Expert Insights on IVDR: Understanding the Impact
With the new In Vitro Diagnostic Medical Device Regulation (IVDR) in place, IVD manufacturers are now subject to much more stringent regulatory requirements and processes, especially when compared to the previous In Vitro Diagnostic Medical Device Directive (IVDD). These new regulations first became effective in 2017 to address key issues identified with the previous regulations. […]
IVDR – Overcoming challenges while establishing Regulatory strategy
By Julia Selmani Regulatory Affairs specialist, Key2Compliance AB Establishing a strategy for regulatory compliance for your company is a new IVDR requirement, defined in Article 10(8a) where the aspects to be addressed by manufacturer’s QMS are listed. Thought ISO 13485 does not explicitly include requirement for Regulatory strategy, it includes the requirement to incorporate regulatory […]
IVDR brings stricter regulations for In Vitro Diagnostic medical devices
In 2016, the European Commission decided to gradually introduce a new mandatory regulatory framework for IVDs: IVDR (In Vitro Diagnostic Medical Device Regulation). The new regulations will replace the old In Vitro Diagnostic Medical Devices Directive IVDD on May 26, 2022. We know that it can be overwhelming to get an understanding of the new […]