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Clinical trial agreements are evolving rapidly as new technologies, regulatory pressures, and workforce challenges reshape how studies are conducted. With many recent regulatory changes and technological advances, today’s teams must balance innovation with compliance while continuing to meet study milestones and accelerate negotiations. Is your organization prepared to adapt and keep trials running smoothly in an increasingly complex environment?
DGE invites you to Philadelphia on August 27–28, 2026 for in-depth, practical discussions on how to leverage homehealth agencies in decentralized trials, navigate global data transfer and cybersecurity requirements, plan for post-trial access, understand the impact of the “One Big Beautiful Bill” on trial participants, strengthen inspection readiness, and MUCH more!
- Clinical Contracts
- Attorneys/Legal/Paralegal
- Clinical Operations
- Clinical Compliance
- Site Development
- Supply Management
- Corporate Counsel
- Technology Solutions
- Contract Manager
- Corporate Counsel
- Clinical Research
- Clinical Analytics
- Clinical Trials
- Medical Operations/Documentation
- Research Practice Manager
- Site Relations
- Regulatory Affairs
- Program Management
- Clinical Development
- Clinical Pharmacology
- Trial Optimization/Trial Design
- Medical Affairs
- Clinical Grants
- Global Clinical Development
- Associate Counsel/General Counsel
- Quality & Compliance
- Clinical Innovation
- Clinical Project Management
- Clinical Trial Supplies
- Medical Director
- Site Budgets/contracts
- Intellectual Property and Litigation
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After the event, all approved presentations are made available exclusively to our valued attendees.*Conditions may apply*
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