Early eMDR Adopters Share Tips On High-, Low-Volume Systems
This article was originally published in The Gray Sheet
Executive Summary
Whether they file 500 Medical Device Reports a year or five, device companies new to electronic MDR reporting should get their feet wet with FDA's eSubmitter and Web Trader tools, industry reps say
You may also be interested in...
eMDR 101: Experts Show Companies The e-Submissions Ropes
Though the date to comply with FDA's new electronic adverse event reporting requirements is still some time away, groups are already gearing up to guide firms through the complex new process
Device Firms Want Two Years To Comply With Electronic MDR Rule
Covidien, AdvaMed and the Medical Imaging and Technology Alliance are asking FDA to give device manufacturers two years to comply with an upcoming rule requiring adverse event reports to be submitted to the agency electronically
Quotable: Words Of Wisdom From Our Recent APAC Coverage
Scrip's APAC team selects notable quotes from recent interviews, conferences and other coverage to highlight the views of senior executives and officials on the major topics facing the biopharma sector in the region.