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Measurement, Analysis, and Improvement for safe and Effective Medical Devices
90 Minutes
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How to Prepare for and Host a FDA Inspection and Respond to 483’s
60 Minutes
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ISO 14971:2019 Medical Device Hazards and Risk Management – All you need to know
90 Minutes
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Trial Master File (TMF) – Clinical Trial Systems and FDA Expectations
60 Minutes
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COVID-19 Update: Get Ready for the HEROES Act’s OSHA Requirements
90 Minutes
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COVID-19 Update: Get Ready for the HEROES Act’s OSHA Requirements
90 Minutes
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Introduction to Design of Experiments
60 Minutes
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3-Hour Virtual Seminar on Human Error Prevention in the Life Sciences
3 Hours
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3-Hour Virtual Seminar on Complaint Handling and Medical Device Reporting and Recalls
3 Hours
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Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Progra
60 Minutes
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Onboarding In A GMP Environment – Best Practices
90 Minutes
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4-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance
4 Hours
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Getting R&D on Board with Risk Analysis
60 Minutes
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FDA’s Latest UDI Labeling Requirements
90 Minutes
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3-Hours Virtual Seminar – Technical Writing for the Regulated Industries
3 Hours
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