Medical Device Regulation,
Implementation Training Course
Are you a regulatory affairs professional, medical device manufacturer, or importer? Do you want to ensure that your devices are compliant with the latest Medical Device Regulation (MDR) requirements?
Join us for a Yashfin’s comprehensive training course that will equip you with the knowledge and skills you need to successfully navigate the MDR certification process. Our expert trainers will guide you through the nuances of the MDR and ISO 13485:2016 requirements, including terminology, documentation, and quality management systems.
Over three days, you’ll learn about:
- The key differences between MDD 93/42/EEC and MDR requirements
- How to develop and implement a Quality Management System (QMS)
- The process for applying for and maintaining MDR certification
- Strategies for managing post-market surveillance and vigilance
Yashfin’s training course is designed to be interactive and engaging, with ample opportunities for networking and knowledge-sharing with your peers. Don’t miss this chance to improve your regulatory compliance knowledge and take your career to the next level.
To register, please complete the registration form below. We’ll be in touch shortly with more information about the course and how to prepare for it.