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GCP Questions, FDA Answers, 2023 Edition
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Gain peace of mind in your next clinical trial with answers to your most pressing compliance questions, and answers to those you might not have even thought of yet, in GCP Questions, FDA Answers. Read More
Research and Development
FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers
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Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
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Designing Secure Medical Devices: Building Cybersecurity into the Development Process
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Statistics and Data for Regulatory Professionals and Attorneys: Product Performance Evidence Made Easy – Webinar Recording/Transcript
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The Biden Administration’s FDA: A Remarkable 2021, What to Expect in 2022 – Webinar Recording/Transcript
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Medical Device Premarket Review Pathways and FDA Mechanisms for Expedited Review – Webinar Recording/Transcript
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Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
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