Case Study: How to Correct an Unexpectedly Difficult GMP Inspection and Prevent a Relapse

One of our clients received an FDA 483 report following an inspection of a European manufacturing facility with significant nonconformances identified, many associated with QC data trails and data integrity. Learn how NSF helped this client avoid a warning letter (through a combination of audit, consultancy and education) and changed the behaviors and mindset that led to the nonconformances.

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