Accelerate Access. Empower Patients. Partner with Industry Leaders.
As Expanded Access, Managed Access, and Post-Trial Access programmes move from optional to essential, biopharma teams are rethinking how they deliver unapproved therapies to patients who need them most - and they can’t do it alone.
From navigating complex global regulations to ensuring supply readiness, managing safety, and capturing meaningful real-world data, operational success hinges on the strength of external partners who understand the stakes and can deliver with precision.
In October, the 4th Operationalise: Early Access Programmes Summit Europe brought together 120+ senior leaders across Access, Clinical Operations, Medical Affairs, Regulatory, and Clinical Supply. These decision-makers weren’t just discussing strategy, they were - and still are - actively seeking expert support to scale access efficiently, compliantly, and globally.
Our Thought Leaders from Pharma and Biotech are Searching for Long-Term Partners to Support Them in:
Regulatory Navigation & Consultancy
Biopharma teams are seeking expert partners who can interpret complex, country-specific regulations, provide guidance on compliance, and streamline approvals for EAPs across global markets.
Clinical Supply & Logistics
With unpredictable demand and non-standard distribution needs, sponsors are looking for flexible, compliant, and responsive supply chain partners who can manage labelling, shipping, and product accountability in early access settings.
Real-World Data & Evidence Generation
Companies are under pressure to collect actionable data without overburdening physicians or compromising compliance with local regulations. They're seeking efficient, compliant data solutions that support evidence needs and downstream regulatory submissions.
Digital Request & Workflow Platforms
Teams want to move away from manual intake and tracking - they need secure, user-friendly digital platforms that streamline request management, consent, reporting, and documentation
Based on Our Research, the Industry is Actively searching for the Following Services:
- Clinical CROs Specializing in EAPs: Expertise in successfully setting up, running, and closing programs
- Clinical Supply Services: Efficiently manage the movement, storage, and supply of resources across countries
- Digital Recruitment Platforms: Facilitate access to and connection with the appropriate patient populations
- EAP Consultants: Provide regulatory guidance and specialised expertise in niche areas of Early Access Programmes
- Data Collection Services and Consultants: Assist in collecting and analysing real-world data from programs
And more!
Explore the Agenda
Discover the key discussions from the summit, including industry breakthroughs and gain exclusive insights during our packed agenda, interactive roundtables, and panel discussions.
Partner With Us
Position yourself alongside other leading solution providers to ensure your brand is at the heart of biopharma deals.
Join Biopharma Experts
Attendees were part of some of the hottest conversations with like‑minded peers across all stages of drug development, forming critical connections through our dedicated networking sessions. We look forward to continuing these impactful discussions and connections at our next event.