Sponsor Responsibilities for Global Drug Studies

State by State Clinical Trial Requirements (Print)

State-by-State Clinical Trial Requirements Reference Guide 2012 (electronic)

Statistical Concepts for Non-Statisticians

Statistical Concepts for Non-Statisticians

Statistical Intuition for Clinical Research Data Managers

Statistical Intuition for Clinical Research Data Managers

Strategies for Active Listening

Strategies for Assessing Risk Tolerance

Strategies for Effective Remote Monitoring

Strategies for Having Difficult Conversations

Strategies for Having Difficult Conversations

Strategies for Managing Difficult Clinical Research Sites

Strategies for Managing Difficult Clinical Research Sites

Strategies for Remote Auditing of Investigative Sites

Strategies for Remote Auditing of Investigative Sites

Study Site Training Series (2018): A 6-Volume Self-Instructional Training Series for Investigative Teams

Study Site Training Series (2018): Volume 1: The Clinical Study Site Team: Roles and Responsibilities

Study Site Training Series (2018): Volume 2: FDA Clinical Research Regulations and GCPs: The Essentials

Study Site Training Series (2018): Volume 3: IRBs/IECs and Informed Consent: Protecting the Rights of Human Subjects

Study Site Training Series (2018): Volume 4: Sponsor Visits and Regulatory Audits: What You Need to Know

Study Site Training Series (2018): Volume 5: Your Role in Reporting Adverse Experiences

Study Site Training Series (2018): Volume 6: Understanding, Evaluating, and Implementing Clinical Protocols