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.
Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.
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Archive: ABCs of GCP and the 13 Principles of ICH GCP E6 -
Archive: Root Cause Analysis: Applying the Concept for Better Study Compliance Management -
Archive: Current FDA and EMA Inspection Findings: Lessons Learned -
Archive: Monitoring Visit Reports for Medical Device Studies -
Archive: Building Relationships with Clinical Research Sites -
Archive: Principal Investigator Oversight and the Appropriate Delegation of Tasks -
Archive: Monitoring Plan Development -
Archive: Coaching Skills for Leaders -
Archive: Adverse Event Monitoring for CRAs -
Archive: Use of Notes to File in Clinical Trial Essential Documentation -
Archive: Preparation, Management, and Response to Inspections and Audits -
Archive: Writing and Updating the Investigator's Brochure -
Archive: FDA Medical Device Approval Process -
Archive: Tools for Trainers: Clinical Research Job-Aids and Checklists -
Archive: Adequate Sponsor Monitoring Systems In Anticipation of FDA Sponsor GCP Inspections -
Archive: Writing and Maintaining the EU Clinical Trial Authorization -
Archive: eTMF Implementation Strategies -
Archive: Data Management in the Electronic Data Capture Arena -
Archive: Case Narrative Writing for Reporting Adverse Events -
Archive: Final AE Regulatory Guidance -
Archive: Quality by Design in Clinical Research: Is This Only for the Protocol? -
Archive: Fraud in Clinical Research: An Overview -
Archive: EMA and FDA Inspections: Key Differences and Similarities -
Archive: Final FDA Guidance: How to Complete the Form FDA 1572
