Medical Device Regulations Under COVID – What You Need To Know 22 September 2020
COVID-19 has challenged the health systems’ dynamics in many ways and industry and regulators have responded by implementing special actions to ensure patients and caregivers are provided with adequate diagnostics, therapies, and protective equipment. In this webinar, Orsola Regaglia and Jean Boudaud will present an overview of the response to COVID-19 from the regulators in key geographies. We will discuss pathways for COVID-related devices regulatory approvals and share our experience with the regulatory review processes.
Presenters: Orsola Regaglia, Consultant and Jean Boudaud, Senior Consultant and Team Lead