eg technology recently attended Medilink’s European Union Advanced Regulatory Affairs for Medical Devices professional development course 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 technology attend conference on the Changes to the Medical Device Regulations in the EU
eg is committed to ensuring all staff are kept up to date with changes in legislation and the most recent industry guidance to help its 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 the team knows will turn its clients’ ideas into compliant and marketable products.
Based in Cambridge, eg technology is a growing product engineering design and development specialist and consultancy. We create the next generation of medical devices and consumer products, making a positive difference to how people live.
We specialise in your products.