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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.
Reinforces its commitment to providing safe, reliable and high-quality supply chain solutions to partners across Europe.
By: Charlie Sternberg
Verge will leverage its platform and proprietary multimodal human tissue data.
By: Patrick Lavery
AMB-104 provides a unique solution to address venetoclax/azacitidine resistance in acute myeloid leukemia (AML).
Experts from the LNP Alliance discuss where LNP programs stall, how the field is moving beyond vaccines, and why translation requires tighter coordination across formulation, characterization, and preclinical testing.
By: Tim Wright
As CGT programs move toward scale, the bigger challenge is no longer capacity alone, but keeping the full supply chain aligned across sites, vendors, and handoffs.
Released By Cryoport Systems
Once operational, the facility will be the company's key drug product facility designed to meet the latest and most stringent requirements for international markets.
Huang brings 25+ years of leadership experience across the pharmaceutical and CDMO sectors.
Breaks ground for a fourth Life Sciences’ aquarius film coatings manufacturing facility in Ambernath, Maharashtra, India.
By: Kristin Brooks
New compact platform combines gel running and imaging for faster nucleic acid verification.
The facility becomes the 18th in WuXi Biologics’ global network.
The manufacturing expansion strengthens domestic supply of Actinium-225.
Expands capacity and capabilities for induced pluripotent stem cell development and manufacturing.
PPS to leverage its North American drug substance facilities to support patient access to Sofdra.
Enhances the company’s ability to support global payload-linker development and manufacturing at its Riverview, Michigan drug substance facility.
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
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