Agenda Archive

Afternoon refreshments, networking and prize draw sponsored by Dr Vince Clinical Research

Identifying latest geopolitical challenges and impact on supply chain
Building contingency protocols from the start of trial to be better prepared for the unexpected
Incorporating risk assessment into project management plans

Leveraging insights of human dynamics to deliver IMP to clinical trials.
Exploring how Clinical Supply Professionals can reinforce a common goal and collaboration that can break down silos.
Bridging the gap between clinical supply, CMC, quality, regulatory, clinical operations and other stakeholders.
Utilizing robust relationships to navigate challenges and enhance trial success.

Setting up a local trial in Sweden: considerations and actions
Communicating with multiple stakeholders
Considering logistical requirements for personalized cell therapy: manufacturing, sites and patients
Providing a small company perspective on cell therapy trial execution

Understand how pharmacovigilance roles and responsibilities align across sponsors, CROs, vendors, and investigators, and why clear roles prevent inefficiencies and issues
Learn how biotech and specialty pharma can develop scalable pharmacovigilance strategies that adapt to dynamic pipelines
Discover how hybrid outsourcing balances in-house oversight with external expertise for global coverage
Explore methods to enhance partnerships so pharmacovigilance can support both compliance and operational delivery
Recognize how a well-designed pharmacovigilance model can accelerate progress from early development to marketing approval