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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FDA's Updated Informed Consent Guidance: WhatEEs New? -
Monitoring Reports: 10 Rules of Effective Report Writing -
Root Cause Analysis: Applying the Concept for Better Study Compliance Management -
ICH E6(R3) and ICH E8(R1) Updates: Impact on Sponsors -
ClinicalTrials.Gov Requirements: Clinical Trial Registration and Trial Results Reporting, Expanded Registry and Results Data Bank -
ICH GCP E6(R3) Updates: Key Changes Impacting Clinical Investigators, Sites, and IND Holders (Sponsor-Investigators and Institutions) -
FDA's February 2025 Guidance Update: Key Changes for IRBs and Clinical Investigators -
Leading Teams in a Changing Clinical Research Environment -
A Systematic Approach to Study Start-Up: Improving Site Activation -
20-Hour Fundamentals of Clinical Research Series: Getting Started in Clinical Research -
Agile Project Management for Clinical Research Data Managers -
30-Hour Design and Conduct of Clinical Trials: Requirements, Statistical Issues, and Clinical Protocols -
12-Hour Clinical Trial Management Series -
Adverse Event Monitoring for CRAs -
9-Hour Regulatory Strategy Development -
Preparing Clinical Research Sites for FDA Inspections -
HIPAA Team Training: Fundamental Training Specifically for Clinical Research Settings -
Negotiation Skills for Clinical Research Professionals -
30-Hour Clinical Data Management On-Boarding Program -
10-Week In Vitro Diagnostic Devices Fundamentals: Study Design, Conduct, Regulatory Requirements and Submissions for Approval -
Creating Impactful Audit Reports in Clinical Research -
The GCPs of Essential Documents -
eTMF Implementation Strategies -
Sponsor Management of Investigator Non-Compliance
