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Welcomes Brian Riley as President and Chief Technical Officer, Joanne Lager, MD as Chief Medical Officer, and Adrian Chaisson as Chief of Staff.
By: Charlie Sternberg
Strengthens its global particle engineering capabilities.
The company is investing $90 million to expand two U.S. facilities to enhance capacity and efficiency.
By: Rachel Klemovitch
Villain offers extensive expertise in peptide and oligonucleotide development and manufacturing.
It is the only ready-to-use liquid immunoglobulin therapy with (IgA) content and is set for commercialization in 2026.
Partnership expected to improve yield and upgrade analytical methods ahead of clinical use and regulatory submissions.
Hervé Hoppenot will retire after 11 years of leading the company through major expansion.
Will develop and commercialize a potential treatment for obesity and metabolic disease based on technology licensed from the U.S. Department of Veterans Affairs.
Addressing increasing complexity, cost of drug development, and navigating regulatory compliance.
By: Kristin Brooks
This strategic partnership provides end-to-end visibility and best-in-class track and trace for Praxis’s customer base.
Mark Foster, General Manager of Oliver Design, shares insights on balancing patient needs, manufacturability, and sustainability in biopharma packaging.
As the pharmaceutical industry continues to evolve, so too does the role of secondary packaging.
Collaboration aims to commercialize a proposed biosimilar of dupilumab across Latin America.
Aim to accelerate the development and commercialization of a novel molecular glue degrader (MGD) program targeting cyclin-dependent kinase 2.
New collaboration aims to optimize a proprietary oral sustained-release dosage form of lenalidomide.
Claims that knock-off drugs sold by telehealth entities and compounding pharmacies are manufactured by foreign suppliers not authorized or inspected by the FDA.
Released By Upperton
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