Changes to Medical Device Regulations in the EU

eg technology recently attended Medilink’s European Union Advanced Regulatory Affairs for Medical Devices professional development course in order to ensure that staff are trained on the new EU regulations and informed of the latest changes in EU legislation. The course covered clinical evaluation, software, human factors and the new regulations.

eg is committed to ensuring all staff are kept up to date with changes in legislation and the most recent industry guidance to help our customers achieve full compliance and understand how this impacts the roles and responsibilities of key stakeholders. This enables eg technology to continue to develop new and innovative products that we know will turn our clients’ ideas into compliant and marketable products.