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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10-Week Establishing a Vendor Qualification and Management Program -
Informed Consent Procedure: Lessons Learned from Inspection Findings -
ABCs of Clinical Research for Clinical Administrative Support Staff -
Approaches to Address Challenges in Vendor Management -
10-Hour Clinical Research Manager Skills Development Series -
ICH GCP E6(R3) Updates: Key Changes Impacting Sponsors and CROs -
ABCs of GCP and the Principles of ICH GCP E6 -
Auditing Sponsors and CROs: Deconstruction and Application of the FDAEEs Compliance Program Guidance Manual -
Strategies for Effective Remote Monitoring -
FDA Drug Approval Process -
Recent Trends in Noncompliance: Critical Review and Analysis of Recent Regulatory Letters and Communications from the FDA, EMA, and Health Canada -
State Laws Governing Clinical Trial Regulatory Compliance -
Risk-Based Auditing: Effective Compliance Strategies -
Key Considerations in Medical Writing: The Clinical Study Protocol, InvestigatorEEs Brochure, Informed Consent Form, and Adverse Events Narratives -
Implementing Quality Agreements -
RECIST 1.0 and 1.1: Overview and Data Challenges in Oncology Clinical Trials -
Overcoming Site Challenges: Managing Sponsor Payment Delays -
30-Hour Clinical Research Auditing Certification Program -
8-Hour Preparing for FDA Bioresearch Monitoring Program (BIMO) Inspections for Drug Safety -
Writing the Clinical Study Protocol -
Identifying Safety Signals in Clinical Trial Data -
12-Hour Statistical Concepts for Non-Statisticians -
Data Quality in Clinical Trials: Rationale and Impact -
Good Clinical Practice: Practical Application and Implementation
