Medical Device Audit and Inspection Training, Compliance Best Practices and Standards

Medical device Audit and Inspection based webinars, in-person seminars, standards and best practices for quality and internal audit professionals in medical device companies - QSR and ISO13485, ICH Q9 and ISO 14971, CAPA, Failure Investigation, Root Cause Analysis, ISO 14971 2007, Internal Quality Audits, Medical Device Process Validation, Standard Operating Procedures, design history file (DHF), device master record (DMR), etc.
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