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Implementing e-Consent for Clinical Trials
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Implementing Risk-Based Verification and Validation
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Informed Consent for Clinical Trials: A Regulatory Reference Guide - 2015 Edition
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Implementing an 11-Step Plan for Device Software Validation and Verification
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Implementing an 11-Step Plan for Device Software Validation and Verification, 2016 Edition
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Guide to the FDA's Financial Disclosure Requirements for Clinical Investigators
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Hack-Proofing Medical Devices: Ensuring Product Safety Through Cybersecurity
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Human Subjects Questions, FDA Answers
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Guide to FDA Medical Device Regulations: 2015 Edition
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Guide to FDA and EU Medical Device Regulations: 2017 Edition - Part 2
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Good Clinical Practices: The New ICH E6 Standard
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Guide to FDA and EU Medical Device Regulations: 2017 Edition - Part 1
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