2025 Full Event Guide
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Operational Excellence in EAPs
Transition & Commercial Readiness
Navigating Regulatory & Compliance Complexity
Overcoming Supply & Logistical Hurdles
- Practical frameworks for designing robust EAP structures
- Aligning internal teams and stakeholders for smooth execution
- Case studies from leading biopharma on real-world programme success
- Preparing for the shift from early access to commercial launch
- Managing supply, site communications, and regulatory notifications
- Ensuring internal alignment for long-term programme sustainability
- Regulatory nuances across multiple markets and EU countries
- Maintaining compliance while enabling rapid patient access
- Integrating governance, quality, and pharmacovigilance standards
- Overcoming global supply and distribution challenges in early access programmes
- Managing labelling, import/export, and regulatory requirements across multiple countries
- Designing scalable and compliant operational processes to maintain programme continuity
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