Ian A Pilcher
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Detailed Analysis
Pilcher's approach to investigations is thorough and strict with emphasis on adherence to regulatory guidelines. He is also focused on understanding the design and changes in the design thoroughly.
Ian A Pilcher is a meticulous FDA auditor with strong focus on adherence to prescribed protocols. He takes keen interest in investigating design validation, risk analysis, handling of complaints, Corrective Action Preventive Action (CAPA) procedures and Medical Device Reporting (MDR) among other things. He is also thorough with the importance of proper documentation and reporting mechanisms to ensure that all internally identified risks are represented accurately.
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