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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Overcoming Site Challenges: Managing Sponsor Payment Delays -
Principal Investigator Oversight and the Appropriate Delegation of Tasks -
Chemistry Manufacturing & Controls (CMC): What Does it Mean? -
Strategies for Having Difficult Conversations -
Utilization of Real-World Evidence (RWE) and Real-World Data (RWD) and Regulations -
10-Week ICH GCP E6: Risk-Based Monitoring Plan Development Series -
Cases in Advanced GCP: A Problem-Solving Practicum -
Regulatory Intelligence -
20-Hour Fundamentals of Clinical Research Series: Getting Started in Clinical Research -
Essential Documentation in Clinical Trials at Research Sites -
Auditing Techniques: A Problem-Solving Practicum -
Investigational Product Accountability Best Practices -
Clinical Trial Start-Up: Using a Work Breakdown Structure (WBS) for Effective Planning -
Managing Phase I Clinical Trials -
Adverse Event Monitoring for CRAs -
Managing CRAs to Improve Performance and Study Outcomes -
18-Hour Writing Clinical/Performance Evaluation Reports -
10-Hour Advanced Clinical Project Management Skills Development -
Statistical Intuition for Clinical Research Data Managers -
Source Documentation: What is Adequate & Accurate? -
ICH GCP E6(R3) Updates: Sponsor Quality Management - Risk-Based/Risk Management Requirements and Approaches for Compliance -
Inspection Readiness: Understanding BIMO Inspection Requirements for Sponsors, CROs, Monitors and Investigators -
Quality Systems: A Controlled Approach to GCP Compliance -
FDA Drug Approval Process
