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Critical Thinking for Clinical Research Professionals - A Companion to DIGR-ACT®
$80.00
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DIGR-ACT® Solution
$399.00
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Comparison Tool: ICH E6(R3) Draft to ICH E6(R2)
$199.00
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GCP Training: ICH E6(R2)
$199.00
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Clinical Trials eSystems Inspection Readiness
$199.00
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Good Clinical Practice Training (GCP): Refresher
$199.00
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ICH E6(R2) GCP Training for Investigator Site Personnel
$199.00
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Corrective and Preventive Action (CAPA) Process Planning for Clinical Research Professionals
$199.00
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HIPAA Training for Clinical Trial Professionals
$199.00
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Overview of ICH E8(R1): General Considerations for Clinical Studies Guideline
$199.00
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Recorded Webinar - Special Considerations in Pediatric Trials
$69.00
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ISO 14155:2020 Medical Device Standard
$199.00
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CRO Oversight
$199.00
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Good Documentation Practices and ALCOA-C
$199.00
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The General Data Protection Regulation (GDPR) and Clinical Trials
$199.00
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Investigator Initiated Clinical Trials
$199.00
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Medical Device versus Drug: Comparing and Contrasting
$199.00
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Clinical Safety Data Management: Definitions and Standards for Expedited Reporting (ICH E2A)
$199.00
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Structure and Content of Clinical Study Reports (ICH E3)
$199.00
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Overview of 21 CFR 312 (IND) and 21 CFR 314 (NDA)
$199.00
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Overview of 21 CFR Part 50 Human Subject Protection and 21 CFR Part 56 IRB/IEC
$199.00
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Overview of 21 CFR 54 Financial Disclosure & Part 11 Electronic Data Signatures
$199.00
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Regulatory Requirements for Clinical Trials in Europe (Directive to Regulation)
$199.00
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Recorded Webinar - A Case for Sponsor Monitoring Remote Access to a Site’s EMR!
$69.00
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Recorded Webinar - Remote Monitoring Operations and Maintaining HIPAA, GCP, and COVID-19 Restrictions Plus FAQ
$69.00