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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Strategies for Remote Auditing of Investigative Sites -
eTMF Quality Oversight: A Risk-Based Approach -
Clinical Research Financial Management for Investigative Sites -
12-Hour Drug Safety and Pharmacovigilance: Effective Drug Safety Reporting and Surveillance -
10-Week CRA & CRC Beginner Program -
Utilization of Real-World Evidence (RWE) and Real-World Data (RWD) and Regulations -
Introduction to Statistics for Non-Statisticians -
10-Week Clinical Research Associate (CRA) On-Boarding Program -
Cases in Advanced GCP: A Problem-Solving Practicum -
Drug Development and FDA Regulations -
Building Quality by Design (QbD) and Risk-Based Quality Management (RBQM) Systems into Clinical Operations -
Establishing Quality Tolerance Limits (E6(R2) and E6(R3)) -
ICH GCP E6(R3) Updates: Impact on Clinical Data Management -
Writing and Updating the Investigator's Brochure -
Principal Investigator Oversight and the Appropriate Delegation of Tasks -
GCP Renovation (ICH E8(R1) and ICH E6(R3)) -
Inspection Readiness: Understanding BIMO Inspection Requirements for Sponsors, CROs, Monitors and Investigators -
EU Clinical Trial Regulation (EU-CTR) Requirements -
Decoding FDA's Draft Guidance on Remote Regulatory Assessments: A Practical Guide -
Monitoring Visit Reports for Medical Device Studies -
Clinical Trial Start-Up: Using a Work Breakdown Structure (WBS) for Effective Planning -
16-Hour Preparing for FDA Postmarketing Adverse Drug Experience (PADE) Inspections for Pharmacovigilance -
Writing the Clinical Study Report -
ICH GCP E6(R3) Updates: Sponsor Quality Management EE Risk-Based/Risk Management Requirements and Approaches for Compliance
