Comparison Tool: ICH E6(R3) Draft to ICH E6(R2)

$199.00

GCP Training: ICH E6(R2)

$199.00

Clinical Trials eSystems Inspection Readiness

$199.00

Good Clinical Practice Training (GCP): Refresher

$199.00

ICH E6(R2) GCP Training for Investigator Site Personnel

$199.00

Corrective and Preventive Action (CAPA) Process Planning for Clinical Research Professionals

$199.00

HIPAA Training for Clinical Trial Professionals

$199.00

Overview of ICH E8(R1): General Considerations for Clinical Studies Guideline

$199.00

ISO 14155:2020 Medical Device Standard

$199.00

CRO Oversight

$199.00

Good Documentation Practices and ALCOA-C

$199.00

The General Data Protection Regulation (GDPR) and Clinical Trials

$199.00

Investigator Initiated Clinical Trials

$199.00

Medical Device versus Drug: Comparing and Contrasting

$199.00

Clinical Safety Data Management: Definitions and Standards for Expedited Reporting (ICH E2A)

$199.00

Structure and Content of Clinical Study Reports (ICH E3)

$199.00

Overview of 21 CFR 312 (IND) and 21 CFR 314 (NDA)

$199.00

Overview of 21 CFR Part 50 Human Subject Protection and 21 CFR Part 56 IRB/IEC

$199.00

Overview of 21 CFR 54 Financial Disclosure & Part 11 Electronic Data Signatures

$199.00

Regulatory Requirements for Clinical Trials in Europe (Directive to Regulation)

$199.00