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International Medical Device Regulatory Monitor
November 2012 | Vol. 20 No. 11
IMDRF Seeks to Harmonize Requirments for Auditors
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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