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WSJ-151/2, Novartis Campus, Basel, CH
As a trusted partner, Novartis Contract Manufacturing offers global cGMP-compliant end-to-end solutions. From Biologics, Fill Finish and Cell & Gene, to mRNA/LNP and Small Molecules (OSD, Peptide and Oligonucleotide), we deliver reliability and quality across Europe, US, and Asia. Scale confidently with our expertise and robust global supply chain.
Partnering to produce high quality, life-changing biotechnological treatments for patients.
Released By Novartis Contract Manufacturing
DNA‑to‑IND offering leveraging GS Ori‑Go designed to deliver tox material in approximately two months, and IND readiness in as little as six months.
By: Kristin Brooks
The facility becomes the 18th in WuXi Biologics’ global network.
By: Patrick Lavery
Will provide microbial contract development and manufacturing services for the recombinant human matrix metalloproteinase-7.
By: Charlie Sternberg
Will support a sustainable path from clinical development to commercial access for therapies serving the smallest patient populations.
How today’s manufacturers are filling the growing need for biologics without rushing complex processes in development or quality control.
Advantages of integrated, QbD-guided formulation development services and key strategies for minimizing risk and maximizing success.
By: Eliza Yeung, PhD
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
Are your perceptions of the CMO marketplace serving your drug program—or holding it back?
Released By AbbVie Contract Manufacturing
How to compare CMO proposals and know what your true costs will be
There are many reasons for a pharmaceutical company to perform a tech transfer to a contract manufacturing organization (CMO).
Epicrispr’s investigational gene therapy, EPI-321, is a treatment for facioscapulohumeral muscular dystrophy.
The partnership will work to advance Novelty Nobility’s bispecific antibody drug candidate through process development and GMP manufacturing.
Expands its capabilities in next-generation biologics with Cizutamig, Candid’s lead investigational asset.
Expansions at sites in both the United States and Europe are crucial to PCI’s vision for the coming years.
Released By PCI Pharma Services
Plans for GMP release for production by the end of 2026.
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