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525 Boulevard Cartier Ouest , Laval, QC, H7V 4A2, CA
Strengthens Ofichem’s integrated development offering, enabling it to offer broader, deeper support from early-phase development through to GMP production.
By: Charlie Sternberg
New suite enables the scalable, diverse, high-quality conjugation services that customers need to advance to the next generation of therapies.
Establishes a Center of Excellence for Aseptic Fill-Finish Processing.
Welcomes Brian Riley as President and Chief Technical Officer, Joanne Lager, MD as Chief Medical Officer, and Adrian Chaisson as Chief of Staff.
Villain offers extensive expertise in peptide and oligonucleotide development and manufacturing.
Will commence cell therapy process development and clinical manufacturing services at AGC Inc.’s Yokohama Technical Center.
Released By Upperton
The expansion will add 9,000 square feet to its Massachusetts facility, expanding development and production capabilities.
By: Rachel Klemovitch
Will support spray drying and unit operations including granulation, encapsulation, compression and coating for oral dosage forms.
How the effectiveness, flexibility and sustainability of single-use technologies solve many of today’s challenges in biomanufacturing.
By: Chris Chen
FUJIFILM Irvine Scientific becomes FUJIFILM Biosciences and FUJIFILM Diosynth Biotechnologies will be known as FUJIFILM Biotechnologies.
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.
By: Tim Wright
New model-based platform is designed to accelerate process development of active pharmaceutical ingredients.
Will add upstream and downstream GMP processing capabilities to meet increasing demand for 2000L scale single-use biologics manufacturing.
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