ANVISA Cancels In Vitro Medical Devices That Failed to Meet Reclassification Deadline
QR Group warns of the impact of non-compliance with the requirements of RDC 36/2015 and guides companies on how to keep their records in compliance In July 2025, ANVISA announced the cancellation of registrations of medical devices for in vitro diagnosis (IVD) that did not meet the deadline for sanitary reframing, established by RDC No. […]
