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Łukasiewicz, known for advanced chemical synthesis and production scaling capabilities, will help ExploRNA ramp up its mRNA manufacturing.
By: Patrick Lavery
The designation applies to the site’s BCM3 antibody intermediate and conjugated drug substance dual-function production line, and DP4 facility.
The 85,000-sq.-ft. East Norriton site adds GMP cleanrooms, fill-finish capacity, and immediate onboarding for cell therapy sponsors.
By: Charlie Sternberg
License variation supports early-phase GMP manufacture at Nottingham facility.
The 3,500-square-meter BIO CITY III facility adds up to 20 cGMP manufacturing lines for cell therapies and personalized medicine.
By: Tim Wright
Deal expands PerkinElmer’s automation, GMP IT and digital manufacturing capabilities for life sciences customers.
Certification supports commercial-scale production of QS-21 and other high-purity saponin fractions for human and veterinary vaccines.
New site will expand lipid-based drug delivery manufacturing capacity.
Drug developers will be able to use 4basebio’s research use only, high-quality, GMP-grade development and clinical programs.
This brings Artis’ U.S.-based development and GMP manufacturing and Spain-based enzymatic synthetic DNA operations under one name.
Why successful technology transfer depends on early planning, process understanding and close collaboration from development through GMP manufacturing.
Released By Upperton
The Research Triangle Park facility supports GMP analytical testing across drug development and manufacturing.
The collaboration supports Restore Vision’s investigational therapy for patients with retinitis pigmentosa.
Agreement covers process development and GMP manufacturing for Plowshare’s AAV-based rare disease program.
New 2,000-square-meter facility expands Merck’s global testing network with commercial drug substance and drug product release testing and GMP-compliant stability studies.
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