Device
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The Medical Device Reporting (MDR) Guidance – An Easily Digestible Compliance BreakdownRita HoffmanOn-Demand00
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00
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00
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FDA Guidance on Medical Device Cybersecurity – Preparing for the Present and FutureDavid KaneOn-Demand00
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20
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00
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00
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00
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Effective Clinical Investigator GCP Training – Getting It Right The First TimeSandra “SAM” SatherOn-demand00
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00
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00
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Good Clinical Practices (GCP) Overview for Clinical Research Professionals – A Global PrimerMichael PierroOn-demand00
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Conducting the CRO Pre-qualification Audit for GCP Compliance – Key Risk Factors to AvoidMichael PierroOn-demand00
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Effective Risk Management & Quality System Implementation for Medical DevicesMarcelo TrevinoOn-demand00