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 11-12, 2027 for in-depth, practical discussions on
how to leverage home health 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!
Featured Topics and Discussions:
- Understand the role of Home Health Agencies in decentralized and hybrid clinical trials
- Navigate global data transfer restrictions and cybersecurity risk
- Plan for post-trial access: ethical and compliance considerations
- Understand the impact of the “One Big Beautiful Bill” on clinical trial participants
- Ensure patient safety in the age of AI
* Clinical Contracts
- 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
- Attorneys/Legal/Paralegal
- Clinical Operations
- Clinical Compliance
- Site Development
- Supply Management
- Corporate Counsel
- Technology Solutions
