Medical Device QMS, ISO 13485 Requirements and CAPA Training, Compliance Best Practices and Standards
Medical device QMS, ISO 13485 and CAPA regulations based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA requirements for medical device QMS, ISO 13485 requirements and CAPA investigations - ISO 13485, Root cause analysis and tools , CAPA, Failure investigation, Effective Hazard Analysis, Internal Quality Audits, Post-Market Surveillance, Equipment calibration, ANSI Z1.4 and ISO 2859, Failure Modes and Effects Analysis, etc.
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