Featured Product In Regulatory Affairs
FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule
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Learn from a prominent regulatory expert how to optimize your LDT applications to help secure a 510k clearance or premarket approval. Read More
Regulatory Affairs
CDRH’s New Accreditation Scheme for Conformity Assessment: Impacts on Your Future Testing Plans and FDA Submissions – Webinar Recording/Transcript
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FDA Digital Health Regulation: Latest Developments for Medical Device Manufacturers – Webinar Recording/Transcript
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Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
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FDA Under the Biden Administration: What’s to Come and What It Will Mean – Webinar Recording/Transcript
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Maintaining Your Risk-Based Cleaning and Disinfectant Programs: Best Practices During COVID-19 – Webinar Recording/Transcript
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Spreadsheet Validation: Best Practices to Maintain Compliance – Webinar Recording/Transcript
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