Área de curso
Disponibilidad
Disponible por 90 días despues de la inscripción
Tiempo aproximado de ejecución del curso
1 hora
Unidades de Educación Continua
0.1
Costo del curso
Sin cargo
El contenido de e-learning está disponible bajo demanda
Detalles del curso
Overview
Over the next few weeks we will be adding five insightful webinars to this page, so please stay tuned as new webinars are published.
These five intuitive webinars will help you focus on various aspects of the MDR, from preparing a Clinical Evaluation Plan, to supporting you with preparing a Clinical Evaluation Report, with an in-depth, 2 - part webinar. Additionally, we’ll also give you advice around preparing a Post Market Clinical Follow Up Plan and Evaluation Report (PMCF) as well as helping you to understand how best to produce a compliant SSCP for both healthcare professionals and patients.
Key takeaways and learning objectives
Topics covered in the Clinical Evaluation Plan Session:
- The MDR Requirements
- Documenting a Clinical Evaluation Plan
- State of the art and defining objectives
- Legacy Device Clinical Evaluation Plans
- Clinical Development Plans
Presenter information
Join Richard Holborow, Global Head of Clinical Compliance, as he talks about preparing for a clinical evaluation plan.
