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Stephenson Building Keele Science Park, Keele, Staffordshire, ST5 5SP, GB
Exploring how CDMO specialization is addressing scalability and making advanced cell-based therapies possible.
By: Tim Wright
Kim offers early three decades of experience across the CDMO, CRO and R&D biopharma sectors.
By: Charlie Sternberg
CDMO will perform HQ plasmid production in support of Phase I/II clinical trials for Infantile Neuroaxonal Dystrophy.
By: Anthony Vecchione
Discussing the use of single-use technologies to improve the biologics manufacturing process.
By: Dr. Kai
Plasmid CDMO alliance supports first gene therapy platform targeting kidney diseases.
Collaboration is focused on restoring vision for people suffering from retinal degenerative diseases with no known cure.
Memphis facility can manufacture clinical (early- and late-phase) as well as commercial cell and gene-modified cell therapies.
By: Kristin Brooks
The new 16,000 sq.-ft. facility is part of Charles River’s efforts to expand its end-to-end capabilities in cell and gene therapy development.
Program aimed to deliver early-stage clinical supply of plasmid DNA for drug substance manufacturing.
To scale manufacturing of second-generation gene therapy for hemophilia A, expanding processes initiated in 2019 to meet ASC clinical program.
Complete production and quality assurance of the plasmids to be used in the GMP production of CG01.
Collaboration investigates enhanced manufacturing of AAV and lentiviral vectors to improve quality and productivity for gene therapy and vaccine developers.
Will increase cell and gene therapy manufacturing capacity, laboratory space, warehousing capabilities and more.
By: Contract Pharma
Collaboration will ensure GMP production of material for Phase I clinical trial of Scancell’s DNA vaccine against SARS-CoV-2.
Sign agreement to secure GMP production of plasmids for production of CG01 gene therapy.
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