The Role of Medical Affairs/Medical Safety in Medical Device Post-Market Risk Assessment & Management
Guide and templates for Medical Affairs input into MedTech Health Hazard Assessment
A Compelling Strategic Role for Medical Affairs in the Context of the new EU MedTech Regulations
This article provides an overview of the new MedTech European regulatory environment and opportunities for the Medical Affairs function to evolve and bring value to the respective organizations.
Podcast: European Union Medical Device Regulations (EUMDR)
This podcast series discusses the basics of EUMDR, what this means more globally (FDA, CFDA) and finally – how we can view this as the golden opportunity to elevate the science of our products and communicate a compelling medical value proposition.