Web Seminars for Clinical Research Professionals
A Barnett Interactive Web Seminar offers you a seamless, secure, multimedia learning experience. These live, instructor-led sessions are designed to be highly interactive, and can be attended by individual attendees or groups at one low cost. No travel, no travel expenses, and no time away from the office!
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Creating Impactful Audit Reports in Clinical Research -
Strategies for Managing Difficult Clinical Research Sites -
10-Week Fundamentals of Drug Development Series -
9-Hour Preparing IND/IDE Submissions: How to Organize, Write, Submit, and Track Submissions -
Trial Master File (TMF) for Sponsors: Set Up and Maintenance -
Monitoring Oncology Clinical Trials -
10-Week ICH GCP E6: Risk-Based Monitoring Plan Development Series -
Mastering Clinical Research Audits: Effective Responses and CAPA Development -
Statistical Intuition for Clinical Research Data Managers -
FDA Medical Device Approval Process -
Incorporating Denials Management into Clinical Research Billing -
Auditing Techniques: A Problem-Solving Practicum -
ICH E8(R1): Changes Impacting Sponsors/CROs -
Managing CRAs to Improve Performance and Study Outcomes -
Writing Pharmacology Sections of an IND Application -
Strategies for Having Difficult Conversations -
ICH GCP E6(R3) Updates: Implementing Risk Management Approaches for Compliance -
FDAEEs Draft Guidance on Integrating Randomized Controlled Trials for Drug and Biological Products into Routine Clinical Practice -
Risk-Based Site Monitoring -
ICH GCP E6(R3) Updates: Overview of Changes Impacting Sponsors, CROs, and Clinical Investigators/Sites -
Research Billing Processing: Leveraging Technology to Maintain Compliance and Mitigate Risk -
10-Week Advanced FDA Post-Marketing Pharmacovigilance Auditing -
Monitoring Plan Development -
Use of Notes to File in Clinical Trial Essential Documentation
