Full Event Guide

Browse the full Event Guide to discover:

  • NAVIGATE the multi-layered regulatory frameworks that require both EMA and country-specific legislation
  • DISCOVER how leading companies are successfully planning, running, closing and reimbursing access programmes across Europe
  • ANSWER your burning questions around drug supply, regulatory harmonisation, and real-world evidence collection
  • BUILD your understanding of the current challenges around reimbursement, integrating of pre- and post-trial access programmes and scoping
  • ENGAGE with your community and peers from leading pharma and biotech companies to build lasting connections, complementary collaborations and improving patient access to life saving drugs
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