An NSF International Company M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Understanding and Preparing for the New EU Regulation (QP)
PrintMedical Devices Module 1
£735 excl VAT (20% discount available for additional delegates booking from the same company)
About this course
The regulatory requirements for medical devices are being revised under a new European medical device regulation. As many decisions are still to be taken this course aims to ensure that you are aware of the most robust and likely requirements to be implemented that have an impact upon your regulatory compliance and future regulatory strategy.
Who Should Attend
Specifically aimed towards quality and regulatory professionals responsible for the formulation of regulatory strategy and ensuring regulatory compliance of medical devices within Europe. For pharmaceutical QPs wishing to understand the regulatory requirements for medical devices including combination products.
CEOs and CTOs of new start-up business will find the modular and flexible delivery of this program of particular interest when formulating a regulatory project plan for their commercialization process.
