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: Introduction to Medicare Coverage Analysis: Impact on Site Revenue Cycles -
Archive: Managing Clinical Trials During the COVID-19 Pandemic -
Archive: Centralized TMF Management: The CRO Sponsor Partnership -
Archive: Investigational Product Accountability Best Practices -
Archive: Risk-Based Auditing: Effective Compliance Strategies -
Archive: Writing the Clinical Study Report -
Archive: Source Documentation: What is Adequate and Accurate? -
Archive: EMA and MHRA Inspections: Successful Planning and Execution Tips and Techniques -
Archive: The IND in a CTD/eCTD Format -
Archive: Sponsor Responsibilities for Global Drug Studies -
Archive: Key Considerations in Medical Writing: The Clinical Study Protocol, Investigator's Brochure, Informed Consent Form, and Adverse Events Narratives -
Archive: HIPAA Team Training: Fundamental Training Specifically for Clinical Research Settings -
Archive: Managing CRAs to Improve Performance and Study Outcomes -
Archive: Auditing Sponsors and CROs: Deconstruction and Application of the FDA's Compliance Program Guidance Manual -
Archive: Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance -
Archive: Informed Consent Procedure: Lessons Learned from Inspection Findings -
Archive: A Systematic Approach to Study Start-Up: Improving Site Activation -
Archive: Use of Electronic Health Record Data in Clinical Investigations -
Archive: Final ICH GCP E6 R2: Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsors-Investigators and Institutions) -
Archive: ABCs of Clinical Research for Clinical Administrative Support Staff -
Archive: Working with Clinical Research Sites: Strategic Planning and Operations for Sponsors and CROs -
Archive: Drug Development and FDA Regulations -
Archive: Risk-Based Monitoring: The Data Management Connection -
Archive: Regulatory Intelligence
