Web Seminar Recordings on Key Clinical Research Topics
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Web Seminar Archives are provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).
Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.
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Archive: Managing Risks in Outsourced Clinical Trials: Practical Approaches and Tools -
Archive: Writing Clinical Study Protocols -
Archive: The GCPs of Essential Documents -
Archive: Data Management Plan Creation: Content and Rationale -
Archive: Protocol Deviations: Documenting, Managing, and Reporting -
Archive: Risk-Based Site Monitoring -
Archive: Monitoring Medical Device Trials: An Introduction -
Archive: Risk-Based Thinking: How Monitors Can Develop an Auditor's Perspective -
Archive: Data Quality in Clinical Trials: Rationale and Impact -
Archive: Case Report Form Design, Strategy, and Standards -
Archive: Good Clinical Practice: Practical Application and Implementation -
Archive: Monitoring Reports: 10 Rules of Effective Report Writing -
Archive: Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada -
Archived: The Revised HHS Common Rule: What You Need to Know Now -
Archive: Cases in Advanced GCP: A Problem-Solving Practicum -
Archive: eTMF Quality Oversight: A Risk-Based Approach -
Archive: Establishing Quality Tolerance Limits -
Archive: Preparing Clinical Research Sites for FDA Inspections -
Archive: Auditing Techniques: A Problem-Solving Practicum -
Archive: Strategies for Effective Remote Monitoring -
Archive: Leading Teams in a Changing Clinical Research Environment -
Archive: Quality Systems: A Controlled Approach to GCP Compliance -
Archive: The CRA Role in Risk-Based Monitoring: Strategies for Effective Remote Monitoring -
Archive: CAP and CLIA Requirements for Clinical Research Laboratories
