Skip to content
Clinical Trial Events
DIA Europe

Talk Additional Sessions track

Closing Session

Thu, Mar 20, 2025 · 2:30–3:45 PM CET San Francisco Room, Congress Center Basel

Speakers

  • Lada Leyens

    Senior Director regulatory · Takeda

    Speaker

  • Monique Al

    Special advisor sr · CCMO, Then Netherlands

    Speaker

  • Sarah Pope Miksinski

    Executive Director, CMC Regulatory Affairs · Gilead Sciences

    Speaker

  • Mark Pellett

    Executive Director · AstraZeneca

    Speaker

  • Gracy Crane

    Policy Lead · Roche

    Speaker

  • Estelle Michael

    Policy and public affairs lead · UCB

    Speaker

  • Claudia Dollins

    Vice President, Precision Medicines, Global Regulatory Affairs · GlaxoSmithKline

    Speaker

  • Thomas Wejs Møller

    Senior Director · Novo Nordisk

    Speaker

  • Sebastian Fischer

    Regulatory Strategy Principal · TÜV SÜD Product Service GmbH

    Speaker

  • Sabina Hoekstra-van den Bosch

    Global Director Regulatory Strategy · TÜV SÜD

    Speaker

  • Wim van der Spuij

    Executive Director, International Patient Safety, Europe · Bristol Myers Squibb

    Speaker

  • James Whitehead

    Head of Patient Safety · Egetis Therapeutics

    Speaker

  • Tim Powell

    Director, Submission Sciences, Global Safety and Regulatory Sciences · Biogen

    Speaker

  • Kate Porch

    Director, elabeling Lead, Global Labeling, Global Regulatory Affairs · Johnson & Johnson

    Speaker

  • Rebecca Lumsden

    Head of Regulatory Science & Policy, Europe · Sanofi

    Speaker

  • Tamara Di Carlantonio

    Regulatory Policy Lead · Roche

    Speaker

  • Inka Heikkinen

    Regulatory Policy Lead, Director · Lundbeck

    Speaker

  • Kostas Papadakis

    Global Head of Oncology Market Access (International) · Bayer

    Speaker

  • Sara Torgal

    Global Regulatory Policy Leader (EMEA) · DIA

    Chair