Edward E Lockwood
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Detailed Analysis
He takes a comprehensive approach towards audit, with a strong emphasis on the practical application of systems and processes. He looks for detailed documentation and diligence in handling nonconformances.
Edward E Lockwood is a meticulous FDA investigator who values rigorous oversight on validation of processes and handling of nonconforming products. He looks for thorough documentation in rework and reevaluations activities, and attentiveness to maintenance scheduling. He also pays particular attention to the complaint handling procedures, especially in relation to how complaints are evaluated for Medical Device Reporting (MDR) reportability.
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