Webinar: How ISO13485 prepares your IVDR Quality System for audits and what it doesn’t cover

With the upcoming IVDR compliance deadline at the end of May, it is crucial to ensure that your organization is fully prepared. Why do so many companies struggle with these requirements, and how can you avoid the most common pitfalls?

Join experienced speakers from Key2Compliance for a deep dive into the challenges companies face and discover strategies to thrive. In this webinar, you will learn:

• How IVDR implementation is supported by ISO13485:2016
• The requirements your quality management system must address that are not covered by ISO13485
• Common obstacles, such as funding, unfeasible manufacturing methods, and building a lean, yet robust, quality management system
• Solutions that can help your company succeed with IVDR compliance
• A live Q&A session where you can ask your questions and get expert advice

Who Should Attend: This webinar is ideal for manufacturers of in vitro diagnostic medical devices, entrepreneurs, business development managers, and anyone involved in product development, regulatory affairs, or quality management within the MedTech industry.