- Recognizing where comparator sourcing typically goes wrong and how those issues affect enrollment, supply, timelines, and cost
- Addressing key challenges such as shelf life, long lead times, country-specific requirements, and blinding needs
- Sharing practical mitigation strategies and lessons learned from real planning scenarios
- Designing compliant multi-language labels across global regions
- Balancing patient-centric packaging with regulatory requirements
- Keeping pace with changing requirements to keep trials moving forward
- Coordinating across regulatory, logistics, and compliance teams to ensure seamless global shipments
- Anticipating geopolitical and policy shifts that impact trade routes and study timelines
- Strengthening communication with regulators, CROs, and suppliers to reduce delays and risk exposure
- Understanding the pharmacy card model
- The program lifecycle: from design to delivery
- A day in the life: sponsor & sites
- Proof of performance: feedback and case studies
- Examining patient and site perceptions of direct-to-participant investigational product shipments
- Understanding how decentralized distribution models influence engagement, site workload and data integrity
- Exploring how AI is supporting trial design, operational efficiency and decision-making across the study lifecycle
