This one-day event will provide you with an overview of the requirements for the concept design phase of a medical device. Plus:
-Assist you in assessing your company’s current readiness for implementing a QMS
-Give you a clear, practical guide to the next steps that you and your company need to take to move through to the next design phase
-Understand the key areas of concept development required
-Gain an overview of the regulatory and quality management system requirements for a concept medical device
-Understand the technical documentation that should be in place for this stage of device development
– Explore early stage risk management and next steps planning
To find out more and to book your place, please click here.