Clinical Quality Oversight
DGE invites you to Philadelphia on September 16-17, 2025, for an in-depth conference designed to help you master risk-based quality management, optimize vendor oversight, enhance audit readiness, adapt to the latest regulatory shifts, and MUCH more![/vc_column_text][/vc_column][/vc_row]
Featured Topics and Discussions:
- Master Inspection Readiness by Learning from Past Patterns
- Delve into the New Revisions for ICH E6(R3) and its Impact on Clinical Research
- Go over the Intricacies Involved in AI Implementation to Improve Quality Analyze Data Integrity and Ensure Data Quality
- Navigate Audit Trail Analytics to Ensure Valid Data
- Manage Vendor and Site Performance to Ensure Quality
- Enhance Diversity in Clinical Trials Through Data-Driven Oversight
- Uncover Specific Challenges Related to Centralized Monitoring
- Strategize Ways to Successfully Implement Change Management in Your Company
Those working for pharmaceutical, biotechnology and medical device companies working in:
- Quality Assurance/ Insights
- Quality Investigation / Analytics
- Monitoring
- Clinical Operations
- Study Optimization / Operations
- Operational Delivery
- Data Monitoring
- Clinical Quality
- Quality Operations
- Central Monitoring/Site Monitoring
- GCP Quality Assurance
- Clinical Data
- Study Monitoring
- Research and Development Operations
- Patient Engagement and Insights
- Quality Oversight
- Risk Management
- Clinical Quality Assurance
- Clinical Development
- Clinical Insights
- Quality Investigation / Analytics
- Medical Quality Systems
- Patient Recruitment
- Clinical Compliance
- Risk Based Quality Management
- Risk Evaluation and Adaptive Integrated
- Clinical Outsourcing / InnovaMon
- Data Management and Analytics
- Clinical Standards
- Clinical Monitoring
- Site Selection
