Good Clinical Practice: ICH E6(R3)

Sale Price:$199.00 Original Price:$249.00

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

$199.00

Critical Thinking for Clinical Research Professionals - A Companion to DIGR-ACT

$80.00

DIGR-ACT Solution

$399.00

Inspection Preparedness for Data Integrity & Governance: Part 11

$199.00

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

$199.00

HIPAA Training for Clinical Research Professionals

$199.00

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

$199.00

Introduction to CRO Oversight

$199.00

ISO 14155:2020 Medical Device GCP Standard

$199.00

Good Documentation Practices and ALCOA+

$199.00

The General Data Protection Regulation (GDPR) and Clinical Trials

$199.00

Considerations for Investigator Initiated Clinical Trials

$199.00

ICH E6(R2) GCP Training for Investigator Site Personnel

$199.00

Good Clinical Practice Training (GCP): Refresher

$199.00

Good Clinical Practice: ICH E6(R2)

$199.00

Recorded Webinar - Special Considerations in Pediatric Trials

$69.00

Medical Device versus Drug: Comparing and Contrasting

$199.00

Clinical Safety Data Management (ICH E2A)

$199.00

Structure and Content of Clinical Study Reports (ICH E3)

$199.00

Overview of 21 CFR 312 IND & 21 CFR Part 314 Post Market Drug Approval

$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

Recorded Webinar - A Case for Sponsor Monitoring Remote Access to a Site’s EMR!

$69.00

Recorded Webinar - Remote Monitoring Operations and Maintaining HIPAA, GCP, and COVID-19 Restrictions Plus FAQ

$69.00