An NSF International Company M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Implementing (QP)
PrintPart of our Medical Devices QP Training Module 1
£1470.00 excl VAT
About this course
A two day implementing course that will allow you to project manage the necessary processes, documentation and registration requirements for a CE marked medical device. Building upon the one day understanding course you will move into establishing the project management steps, milestones, procedures and regulatory interactions necessary to successfully coordinate a CE marking project.
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.
