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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Developing and Negotiating Research Site Clinical Study Budgets and Contracts -
FDA's Draft Guidance on Ethical Considerations for Clinical Investigations of Medical Products Involving Children -
Current FDA and EMA Inspection Findings: Lessons Learned -
CRO Partnership Management -
Auditing Clinical Research Studies: An Overview for Assessing GCP Compliance -
Managing Risks in Outsourced Clinical Trials: Practical Approaches and Tools -
Source Documentation: What is Adequate & Accurate? -
Strategies for Active Listening -
15-Hour Clinical Trial Assistant Fundamentals Training Program -
ICH GCP E6(R3) Updates: Impact on Clinical Data Management -
Becoming a Clinical Research Investigator: Roles, Responsibilities and Successful Clinical Trial Management -
Working with Clinical Research Sites: Strategic Planning and Operations for Sponsors and CROs -
GCP Renovation (ICH E8(R1) and ICH E6(R3)) -
Coaching Skills for Leaders -
Risk-Based Quality and Compliance Management in Combination Product Trials -
EU Guideline on Computerised Systems and Electronic Data in Clinical Trials -
30-Hour Clinical Project Management Fundamentals Certification Program -
ABCs of GCP and the Principles of ICH GCP E6 -
ABCs of Clinical Research for Clinical Administrative Support Staff -
The CRA Role in Risk-Based Monitoring: Strategies for Effective Remote Monitoring -
Technology Innovation and Intellectual Property (IP) in the Biomedical Industry -
Building Relationships with Clinical Research Sites -
Developing Clinical Study Budgets for Sponsors -
Risk-Based Monitoring and Quality Management of Clinical Trials: Recent Guidance Updates from the FDA and EMA
