Professional Certificate in Medical Device Documentation and Reporting
-- ViewingNowThe Professional Certificate in Medical Device Documentation and Reporting is a comprehensive course designed to meet the growing industry demand for experts in medical device documentation. This certificate equips learners with critical skills necessary for career advancement in this field.
5,700+
Students enrolled
GBP £ 140
GBP £ 202
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Here are the essential units for a Professional Certificate in Medical Device Documentation and Reporting:
• Introduction to Medical Device Documentation: Understanding the regulatory landscape, types of medical device documentation, and their importance in product development and commercialization.
• Design Control and Documentation: Designing and documenting medical devices according to FDA and ISO standards, including design inputs, outputs, and verification/validation activities.
• Risk Management and Documentation: Implementing risk management processes and documenting risk assessments, mitigation strategies, and residual risks.
• Manufacturing and Quality Control Documentation: Establishing and documenting manufacturing processes, quality control procedures, and deviations.
• Complaint Handling and Reporting: Implementing complaint handling processes and reporting adverse events to regulatory authorities.
• Clinical Evaluation and Reporting: Conducting clinical evaluations, analyzing clinical data, and reporting results to regulatory authorities.
• Post-Market Surveillance and Reporting: Monitoring and reporting post-market surveillance data, including product performance, customer feedback, and adverse events.
• Medical Device Documentation Management System: Implementing a documentation management system for medical devices, including document control, version control, and security.
• Auditing and Inspection Preparation: Preparing for and undergoing audits and inspections by regulatory authorities and notified bodies.
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