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Home » CDRH Will Develop New MDR Database Rather Than Transitioning to AERS
CDRH Will Develop New MDR Database Rather Than Transitioning to AERS
November 19, 2010
CDRH has canceled its plan to move medical device reports (MDRs) to the FDA’s adverse event reporting system (AERS) by year’s end in a move that could delay the mandatory electronic submission of MDRs.