论文信息 - FDA Regulations and Auditing Practices for Software Suppliers at a Pharmaceutical Manufacturer

FDA Regulations and Auditing Practices for Software Suppliers at a Pharmaceutical Manufacturer

A review of 17 quality audit reports performed between 1992 and 2003 by an international pharmaceutical company identifies three time frames of audit maturity based on government regulation enforcement patterns, supplier quality practices, and the custo..

Colin J. Neill | Theisen | W Timothy

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