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60 Langiewicza , Konstantynów Łódzki, Łódzkie, 95-050, PL
Mabion is a fully integrated CDMO offering a wide services associated with the development and GMP manufacturing of biotherapeutics, including mAbs and vaccine antigens. Mabion offers an end-to-end solution, covering all stages of biologic drug development from CLD through process scale-up and analytics to sterile fill and finish and QC release.
This will support the advancement of a novel ophthalmic therapeutic through clinical development and onto the market.
By: Rachel Klemovitch
The Fosun Pharma-Teva collaboration agreement aims to accelerate clinical data generation for TEV-56278 and develop Anti-PD1-IL2 Therapy.
Purolite AP+50 is an affinity chromatography resin designed to help achieve cost savings and optimize operations throughout the antibody manufacturing process.
By: Charlie Sternberg
The purpose-built 200,000-square-foot plant will serve as innovation hub and location for future capabilities expansions.
The research program will combine Debiopharm’s AbYlink conjugation technology with Alkyon’s modular antibody platform and novel targeting approaches to advance targeted radiopharmaceutical treatments.
The all-stock transaction will build on BioNTech’s proven track record and established position in the global mRNA industry.
Dick is an experienced operations executive with over 30 years of experience in project and line management.
The ExPERT and IRO platforms were integrated to improve the yield of gene-edited T cells and shorten manufacturing timelines.
The companies partner on antibody drug conjugates, drug substance, and drug product manufacturing services.
Partnership includes joint research, technology transfer, and co-development of lead candidates.
The collaboration will create a path from concept to preclinical development of complex diseases in the Biopharmaceutical Industry.
Glycovax has refined its production to meet regulatory requirements and will market the protein through its subsidiary Espoir Therapeutics.
The new facility will be built next to the existing Lukácsháza site.
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.
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