By Angela Osborne2023-06-06T12:00:42
CDMOs have been squeezed by the sharp increase in companies preparing to scale their cell and gene therapy manufacturing for Phase III trials and commercialisation, and physical capacity has been a common scapegoat. But eXmoor CEO Angela Osborne says the real limiting factor is experience.
Already a member? Sign-in
European Pharmaceutical Review delivers authoritative insights, cutting-edge innovations, and expert perspectives that not only inform decisions but drive measurable progress across quality, compliance, and operational excellence.
By becoming a member you join a connected and collaborative community driving the industry forward. Member benefits include:
2026-04-29T14:00:00Z 2026-04-29T15:00:00Z
Sponsored by USP
2026-05-27T14:00:00Z 2026-05-27T15:00:00Z
Sponsored by TA Instruments
2026-04-16T15:00:00 2026-04-16T16:00:00
Sponsored by Thermo Fisher Scientific
2025-11-20T15:00:00
Sponsored by Rapid Micro Biosystems
2025-09-19T15:55:00
Sponsored by Sartorius, By Marko Narobe (Sartorius Biosepartions), Michael Gerrero (BridgeBio) and Srivatsan Ramesh (BridgeBio)
2026-03-04T15:00:00 2026-03-04T16:00:00
Sponsored by METTLER TOLEDO
Site powered by Webvision Cloud