Medical Device Documentation and Data Management Regulations Training, Compliance Best Practices and Standards
Medical device documentation and data management regulation based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA medical device documentation requirements and regulations governing data management to ensure compliance - 510(k) submissions, Design History Files, Device History Records, Device Master Records, Software Verification and Validation, IEC 62304, Mobile medical applications, etc.
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