The IVDR transition deadline is approaching Incomplete Technical Documentation submissions are one of the most common reasons for delays to the certification process. To make the process more efficient for you, access the key resources you need to help you prepare. IVDR Transition Toolkit Register for our next webinar on Performance Evaluation under the In Vitro Diagnostic Regulation on 26 August at 09:00 BST and 16:00 BST Conformity assessment routes recorded webinar Conformity assessment routes brochure Listen back to our IVDR application process and QMS for IVDR webinars New Active Implantable Devices brochure  As one of the highest risk categories of device, Active Implantable Medical Devices (AIMDs) are subject to rigorous regulatory controls before they can reach global markets. It is critical to work with a notified body that understands the industry and has the experience to review and confirm your products’ readiness for market – efficiently, reliably and promptly. Talk to …