Featured Product In Quality
Medical Device Risk Management Tools — FMEA Does Not Equal Risk Assessment
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Learn how to properly assess, reduce and manage risks associated with your medical devices and comply with ISO 14971 with the Medical Device Risk Management Tools — FMEA Does Not Equal Risk Assessment management report. Read More
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Inspection Readiness for EU GMP Annex 1 – Manufacture of Sterile Medicinal Products – Webinar Recording/Transcript
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FDA in 2024 and Beyond: What Election-Year Changes Mean for Your Business – Webinar Recording/Transcript
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Managing Data and Documentation for FDA Inspections and Remote Assessments – Webinar Recording/Transcript
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FDA as a Development Partner: A New Approach to Product Review Meetings – Webinar Recording/Transcript
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