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Home » IMDRF Seeks to Harmonize Requirments for Auditors
IMDRF Seeks to Harmonize Requirments for Auditors
November 2, 2012
Organizations that audit device establishments must ensure that their findings document conformity, nonconformity or potential nonconformity with established best practices based on objective evidence, according to a draft standard released by the International Medical Device Regulators Forum (IMDRF).
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