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The collaboration integrates LenioBio’s cell-free protein expression platform with Twist’s DNA manufacturing and automation capabilities.
By: Patrick Lavery
The comprehensive on-site inspection was conducted April 14.
Rengis brings extensive international leadership experience across pharmaceutical manufacturing, R&D and CDMO operations.
By: Charlie Sternberg
How today’s manufacturers are filling the growing need for biologics without rushing complex processes in development or quality control.
By: Kristin Brooks
Advantages of integrated, QbD-guided formulation development services and key strategies for minimizing risk and maximizing success.
By: Eliza Yeung
Integrated approach simplifies development, reduces risk, and supports scalable manufacturing.
How Pfizer CentreOne helps customers navigate complexity in OSD manufacturing through a consistent network and targeted technical expertise at the site level.
Released By Pfizer CentreOne
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
There are many reasons for a pharmaceutical company to perform a tech transfer to a contract manufacturing organization (CMO).
Released By AbbVie Contract Manufacturing
Epicrispr’s investigational gene therapy, EPI-321, is a treatment for facioscapulohumeral muscular dystrophy.
The companies will use Cellular Origins’ automated mobile robotic platform.
The new line of high-clarity PETG bottles is designed to support the demanding requirements of pharmaceutical and biopharmaceutical manufacturing environments.
The collaboration combines HAS Group’s expertise in complex bioconjugation, process development, and clinical-grade manufacturing with Biodelphis Therapeutics’ APIC platform.
Will further advance U.S.-based production capacity, enhance next-gen technologies and support a reliable supply of medicines for patients.
The partnership will work to advance Novelty Nobility’s bispecific antibody drug candidate through process development and GMP manufacturing.
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