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 the 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
EARLY BIRD DISCOUNT: book your place before 5pm on Friday 18 January and members will pay £160 and non-members will pay £240
Member cost: £200
Non-Member cost: £300
All prices are subject to VAT
Once we have received your booking form, you will receive a confirmation email and an invoice will follow.