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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
The MDSAP Audit Process: Latest Developments and Best Practices – Webinar Recording/Transcript
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Consumer Diagnostics and Wellness Testing: Navigating the Medical Device Regulations – Webinar Recording/Transcript
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Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
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CDRH’s Proposed Rule Harmonizing QSR and ISO 13485: Everything Devicemakers Must Know and Do to Prepare – Webinar Recording/Transcript
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Medical Device Regulatory Policy: Breakthrough Technologies, STeP and — Wait for It — Reimbursement – Webinar Recording/Transcript
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Spreadsheet Validation: Best Practices to Maintain Compliance – Webinar Recording/Transcript
$287.00
The Biden Administration’s FDA: The First Six Months and What to Expect for the Rest of the Year – Webinar Recording/Transcript
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Demystifying AI in the Life Sciences Industry: What Regulatory, Quality and Compliance Professionals Need to Know – 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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CDRH’s New Accreditation Scheme for Conformity Assessment: Impacts on Your Future Testing Plans and FDA Submissions – Webinar Recording/Transcript
$287.00