Clinical Trials & Good Clinical Practices (GCP) Training
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Writing Clinical Monitoring Reports: Using the Liquid Report Writing MethodSandra “SAM” SatherOn-demand00
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Source Data Review (SDR) vs. Source Data Verification (SDV) – A Site Monitoring Best Practices UpdateSandra “SAM” SatherOn-demand00
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Remote Monitoring Implementation Post ICH GCP E6 (R2): A Practical GuideSandra “SAM” SatherOn-demand00
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The Power of Influencing – Achieving Patient-focused Outcomes to Guarantee SuccessJill DonahueOn-demand00
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Authoring and Implementing Standard Operating Procedures (SOPs): Best Practices for SuccessJoanna GallantOn-Demand00
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Document Authoring, Archive, and Inspection – Challenges And Tips For Establishing Audit-Proof ProcessesDaniel Orfe, Betsy FallenOn-demand00
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Understanding The New NIH/HHS Final Rule On Clinical Trial Reporting – Tips For Compliance SuccessMichael PierroOn-demand00