Clinical Trials & Good Clinical Practices (GCP) Training
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The Impact of “Brexit” On Clinical Research – An Operational Readiness PrimerMichael PierroOn-Demand00
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Conducting an Effective GCP Audit of a CRO-Managed Ongoing Study: Tips and SuggestionsMichael PierroOn-Demand00
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Investigator Oversight Plans: Essentials for Inspection Readiness Post ICH GCP E6 (R2) AddendumSandra “SAM” SatherOn-Demand00
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CAPA and Root Cause Analysis: Essentials Post ICH GCP E6 (R2) AddendumSandra “SAM” SatherOn-Demand00
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Certified Copies and ALCOA-C: Essentials Post ICH GCP E6 (R2) AddendumSandra “SAM” SatherOn-Demand00
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Monitoring Electronic Health Records (EHRs): Frequently Asked Questions – Understanding the Recent May 2016 FDA Draft GuidanceSandra “SAM” SatherOn-demand00
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Good Documentation Practices for Clinical Trials – Ensuring Air-Tight ResultsSandra “SAM” SatherOn-demand00