The world of Medical Device and In Vitro Diagnostic regulations is complex. Your team need to understand the entire process, from inception to placing on the market and how you incorporate a Quality Management System into your business. Our team of experienced consultants are here to help you understand the regulations and requirements of medical device and cosmetic registration to ensure you not only become compliant but stay compliant as legislation, standards and expectations change regularly.
How is training delivered?
Training services are bespoke to the client’s needs. Our objective is to give your team all of the skills they need to ensure your devices are compliant. We can conduct training either virtually or onsite
Our sessions can cover
Risk Management
ISO 13485
EU MDR, EU IVD or UKCA implementation
Creation of Technical Documentation and much more
