MedilinkWM in conjunction with Acclaim Biomedical Consulting is offering a one day workshop exploring the requirements needed for software development and manufacturing within Medical Devices.

This course will focus on the regulatory requirements that surround the software that is used and needed in Medical Devices and manufacturing environments, touching on the associated standards and how to ensure compliance, with a particular focus on risk management and software lifecycles. You will also explore how ISO 62366, ISO 62304 and ISO 60601 impacts on software processes and usage and review what regulators will be looking for.

Delegate Fee:
Receive a 15% discount when booking before Friday 29th January 2016
Member Fee: £140 + VAT
Non-Member Fee: £190 + VAT

Click here for more information.