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Live Courses/Webinars
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Clinical Trials (GCP)
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Medical Devices
Regulatory
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DIGR-ACT: Critical Thinking Skills for Clinical Trials
LSTI Learning Library
Training Voucher Packages
Checkout
Custom Training
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The Medical Device Reporting (MDR) Guidance – An Easily Digestible Compliance Breakdown
Rita Hoffman
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$279
The New Medical Device Single Audit Program (MDSAP) for Manufacturers – Analyzing Rewards and Challenges
Marcelo Trevino
On-demand
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Device Compliance Audit Management – Best Practices to Meet Global Regulations and Notified Body Expectations
Marcelo Trevino
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Medical Device Complaint Handling and MDR Reporting
Dan O’Leary
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