- Valuation of clinical items moving through borders
- HS/HTS codes for blinded clinical shipments versus clinical supplies moving to distribution sites
- VAT expenses: how they apply, when and how they can be recovered
- Sanctions and exemptions in the pharmaceutical industry
- Overall best practices to approach your clinical studies from a customs perspective
- Establishing cross functional teams early to strengthen supply chain performance
- Implementing agreements and team charters to support effective collaboration
- Improving clinical supply chain management and trial timelines through alignment
- 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
