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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.
Plans an expansion of its flagship biologics manufacturing facility in Frederick and construction of a new facility in Gaithersburg.
By: Charlie Sternberg
Codis launches as a global CDMO specializing in spray drying, amorphous solid dispersions, and particle engineering, uniting Particle Dynamics and EUROAPI’s former Haverhill facility under one brand.
Released By Codis
Sentry’s foreign trade zone expertise helps pharmaceutical companies mitigate risks from tariffs and global trade volatility.
Released By Sentry BioPharma Services, Inc.
AGC Biologics to provide GMP manufacturing for AAVantgarde’s two novel candidates designed to address progressive and irreversible vision loss.
The strategic investment will help ensure all key Novartis medicines for U.S. patients are manufactured in the U.S. and delivered to patients across the country at scale.
David Basile of Hovione discusses expanded spray drying capacity in East Windsor and the benefits of integrated development, scale-up, and manufacturing at a single U.S. site.
Released By Hovione
Underscores the facility’s dedication to upholding the highest standards of quality across operations.
A conversation with Upperton’s Director of Pharmaceutical Sciences
Released By Upperton
To provide access to dedicated, fully equipped wet lab facilities and strategic scientific engagement.
By: Kristin Brooks
Enables efficient nucleic acid purification, helping researchers to move faster from sample to PCR testing.
New program is designed to provide financial support to Japanese academic research with the goal of accelerating the translation of innovation into novel therapies for patients.
This is the world’s first liquid formulation of IV infliximab and is available in 100 mg and 350 mg vials.
By: Rachel Klemovitch
The financing will help the company further develop its drug discovery platform.
Richard Pazdur to help guide CDER agenda to modernize the agency and streamline the approval process.
Over the past 20 years, the company has grown from a small startup into a trusted CDMO partner for biopharma companies worldwide.
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