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Unit 1/Chancellor Court , Suite 335, Guildford, GU2 7AB, GB
Glycovax has refined its production to meet regulatory requirements and will market the protein through its subsidiary Espoir Therapeutics.
By: Rachel Klemovitch
Investment enables GL CHEMTEC to provide preclinical and first-in-human offerings.
This adds to BioDlink's portfolio of international GMP approvals, following recent certifications in Brazil, Indonesia, Egypt, and Colombia.
Makes strategic investments in injectable packaging and cold chain capabilities in the U.S. and Europe.
By: Charlie Sternberg
Confirms the site’s full compliance with current Good Manufacturing Practices (cGMP).
The IDMO Smart Factory will enable scalable and cost-effective cell therapy manufacturing.
CEO Owen Murray on driving innovation with high science and high service.
By: Tim Wright
Industry experts weigh in on current trends, challenges, and the future of the cell and gene therapy CDMO market.
ATP-bioluminescence and regulatory advancements address unmet manufacturing and testing needs.
How the effectiveness, flexibility and sustainability of single-use technologies solve many of today’s challenges in biomanufacturing.
Cryoport Systems is transforming the advanced therapies supply chain with integrated services that support every stage of development from early clinical to commercial scale.
Released By Cryoport Systems
Sterling will manufacture cGMP clinical material for KIVU-107 at its bioconjugation facility in Deeside, UK.
The CDMO's head of development talks about ADCs, accelerated timelines, and the push for end-to-end development services.
Aim to support the advancement of cutting-edge cell therapies.
Will add upstream and downstream GMP processing capabilities to meet increasing demand for 2000L scale single-use biologics manufacturing.
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