Products

Clinical Project Management: Fundamentals of Project Management

Clinical Trial Assistant Fundamentals

Clinical Trial Start-Up: Effective Planning for Sponsors, CROs, and Sponsor-Investigators

Clinical Trial Start-Up: Using a Work Breakdown Structure (WBS) for Effective Planning

Coaching Skills for Leaders

Comprehensive Monitoring for Medical Devices

Conducting Clinical Trials Under ICH GCP E6

Corrective Action Plans: Essential Documentation of a SiteEEs Response to GCP Deficiencies

CRA & CRC: Beginner Program

CRA Training Series: A 7-Volume CRA Self-Study Curriculum (2018)

CRA Training Series: Volume 1 - An Overview of Drug Development (2018)

CRA Training Series: Volume 2 - Identifying and Screening Investigators (2018)

CRA Training Series: Volume 3 - Conducting the Prestudy Visit (2018)

CRA Training Series: Volume 4 - Conducting the Study Initiation Visits (2018)

CRA Training Series: Volume 5 - Conducting Routine Monitoring Visits (2018)

CRA Training Series: Volume 6 - The CRA's Reference for Adverse Events (2018)

CRA Training Series: Volume 7 - Test Your CRA Knowledge (2018)

Current FDA and EMA Inspection Findings: Lessons Learned

Data Quality in Clinical Trials: Rationale and Impact

Database Design Considerations in Clinical Trials

Decoding FDA's Draft Guidance on Remote Regulatory Assessments: A Practical Guide

Developing and Negotiating Research Site Clinical Study Budgets and Contracts

Developing Clinical Study Budgets for Sponsors