This one-day course by Medical Device Consultancy will cover Regulatory insights into Medical Device Software. Find out what you need to do to comply with regulation, and work with the experts to plan how you are going to do it.
Learning outcomes will include:
•Understand what software is, and what the essential requirements are according to the MDD and MDR
•Understand FDA requirements for software, how it is classified and regulated
•Write a rationale for classification of an application under the MDD and MDR
•Outline an action plan for software compliance in your organisation
Member cost: £200
Non-Member cost: £300
All prices are subject to VAT.
Once we receive your booking form, you will be sent a confirmation email and an invoice.