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).
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Archive: Subject Recruitment: Proactive Project Plans and Issues Management -
Archive: ICH E6(R3) and ICH E8(R1) Updates: Impact on Sponsors -
Archive: RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials -
Archive: ICH GCP E6(R3) Updates: Sponsor Quality Management - Risk-Based/Risk Management Requirements and Approaches for Compliance -
Archive: ICH GCP E6(R3) Updates: Impact on Clinical Data Management -
Archive: ICH GCP E6(R3) Updates: Overview of Changes Impacting Sponsors, CROs, and Clinical Investigators/Sites -
Archive: FDA Drug Approval Process -
Archive: Inspection Readiness: Understanding BIMO Inspection Requirements for Sponsors, CROs, Monitors and Investigators -
Archive: Monitoring Oncology Clinical Trials -
Archive: Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2 -
Archive: ICH GCP E6(R3) Updates: Key Changes Impacting Sponsors and CROs -
Archive: FDA Requirements for Electronic Source Data in Clinical Investigations -
Archive: FDA's Updated Informed Consent Guidance: What's New? -
Archive: Introduction to Clinical Research -
Archive: Strategies for Having Difficult Conversations -
Archive: Strategies for Managing Difficult Clinical Research Sites -
Archive: Introduction to Data Management -
Archive: Essential Documentation in Clinical Trials at Research Sites -
Archive: Implementing Quality Agreements -
Archive: EU Clinical Trial Regulation (EU-CTR) Requirements -
Archive: ICH E6 (R3) Draft: A Discussion -
Archive: Good Clinical Practice (GCP) for Medical Devices: ICH GCP E6 and ISO 14155 -
Archive: GCP Renovation (ICH E8 R1 and ICH E6 R3) -
Archive: Developing and Negotiating Research Site Clinical Study Budgets and Contracts
