An NSF International Company M1 - CE & Global Regulatory Professional - CE Marking Requirements for Medical Devices – Complex Borderline and Class III Medical Devices (QP)
PrintMedical Devices Module 1
£735 excl VAT (20% discount available for additional delegates booking from the same company)
About this course
Class III and borderline medical devices falling under the medical devices CE marking regulatory requirements require a knowledge of a higher level of interaction with the notified body, competent authorities and other regulatory agency expert groups. From preclinical, clinical and regulatory specifics associated with Class III products we enable you to understand the specific regulatory hurdles that you need to clear prior to successful CE registration.
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.
