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152 Avinguda de la Generalitat , Sant Cugat del Vallès, CT, 08174, ES
Grifols Partnership is a CDMO focused on added value injectable products, with a large international experience in the development and manufacturing of sterile drug products (small molecules) in glass vials and PP bags. Strict compliance with global manufacturing standards has earned us the highest accreditations, including authorizations by the U.S. FDA, EU and U.S. GMP and authorization for parametric release sterility.
As trade policy, regulatory scrutiny, and capital discipline reshape biologics development, sponsors are rethinking where and how commercial manufacturing is secured. Bora Biologics’ recent U.S. expansion and validated 2,000L scale-up reflect a broader shift toward demand-aligned, inspection-ready commercial capacity in the markets where products will ultimately be supplied.
Released By Bora Biologics
Epicrispr’s investigational gene therapy, EPI-321, is a treatment for facioscapulohumeral muscular dystrophy.
By: Patrick Lavery
Will further advance U.S.-based production capacity, enhance next-gen technologies and support a reliable supply of medicines for patients.
By: Charlie Sternberg
The new API facility in North Carolina will enable end‑to‑end manufacturing for all advanced technology platforms in U.S.
This week, Contract Pharma visited an expanding New Jersey facility, and launched a new audience service.
After Sandoz boards the J.Train, Just-Evotec launches continuous ‘facility blueprint.’
By: Dan Stanton
Method transfer completed at Adare’s Vandalia, Ohio facility; first engineering batch produced.
The new center strengthens Ecolab’s life sciences footprint.
Aim to accelerate early-stage biotech innovation in Asia-Pacific.
New site will focus on developing complex generic inhalation products for the EU/UK market and APAC market.
This article examines the pros of building a biorepository in-house compared to the pros of buying a biorepository through an outsourced partner.
Released By Thermo Fisher Scientific Pharma Services
Expands downstream fermentation capacity to support contract manufacturing services for drug substance business.
By: Kristin Brooks
The single-tablet regimen of doravirine and islatravir will be available in U.S. pharmacies as soon as May 12.
Enables AskBio to advance its REGENERATE-PD Phase II trial in the U. S. with the material produced at its subsidiary, Viralgen's commercial manufacturing facility.
Further advancements in Europe and the US increase capacity and process efficiency.
Released By Vetter Pharma International
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