DeviceWeek, 4December 2020 MedWatch Question About 3rd-Party Servicers Slides Under Industry's Radar

On this week’s podcast: A change made by the US FDA to its MedWatch program that asks adverse event reporters whether a third party serviced a malfunctioning medical device went unnoticed by many in industry for nearly a year. We explain why, and tell how the servicer question will be helpful for manufacturers and the agency. Medtech Insight article addressing topics discussed in this episode: • Recent eMDR Change By FDA Asks Adverse Event Reporters About Third-Party Servicers https://medtech.pharmaintelligence.informa.com/MT142951/Recent-eMDR-Change-By-FDA-Asks-Adverse-Event-Reporters-About-Third-Party-Servicers