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!
-
Database Design Considerations in Clinical Trials -
Establishing Quality Tolerance Limits (E6(R2) and E6(R3)) -
Managing Successful Pre-IND/IDE Meetings with the FDA -
Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada -
Building Quality by Design (QbD) and Risk-Based Quality Management (RBQM) Systems into Clinical Operations -
ICH E8(R1): Changes Impacting Sponsors/CROs -
10-Hour Clinical Research Manager Skills Development Series -
ICH E6(R3) and ICH E8(R1) Updates: Impact on Sponsors -
Preparation, Management, and Response to Inspections and Audits -
Writing Toxicology Sections of an IND Application -
Drug Development and FDA Regulations -
Overseeing Teams and Projects -
ICH E8(R1): Designing Quality into Clinical Studies -
30-Hour Clinical Project Management Fundamentals Certification Program -
Writing and Updating the Investigator's Brochure -
16-Hour Preparing for FDA Postmarketing Adverse Drug Experience (PADE) Inspections for Pharmacovigilance -
10-Week Clinical Research Associate (CRA) On-Boarding Program -
The IND in a CTD/eCTD Format -
Strategies for Effective Remote Monitoring -
EU Clinical Trial Regulation (EU-CTR) Requirements -
Understanding ICH E6(R3) (GCP) Updates: Key Changes from R2 -
Auditing Sponsors and CROs: Deconstruction and Application of the FDA's Compliance Program Guidance Manual -
10-Week Fundamentals of Drug Development Series -
FDA's February 2025 Guidance Update: Key Changes for IRBs and Clinical Investigators
