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250 Frankfurter Straße, , Darmstadt, HE, 64293, DE
In this guidebook, experts share key considerations for biopharmaceutical companies as they advance their antibody drug to commercial manufacturing.
Released By MilliporeSigma
The ability to monitor biopharma processes in real time provides significant advantages in optimizing product quality with respect to multiple attributes.
In such a rapidly changing environment, it’s more important than ever to know who you can rely upon to help you succeed.
MilliporeSigma unveils its new Mobius® iFlex Bioreactor family for fed-batch and perfusion upstream processes.
How do sponsors and CMOs realize the advantages of their partnership while avoiding the pitfalls of clunky data sharing?
This whitepaper spotlights how excipient combinations can enhance manufacturability and final concentration of mAb formulations.
This automated approach minimizes the number of human interventions needed and reduces the risk of contamination and batch failures.
The Pellicon® Capsule is the first of its kind—a true single-use TFF device that streamlines bioprocessing with its innovative, simplified design.
This white paper describes key considerations and provides guidance on the preparation of a coating formulation.
MilliporeSigma's new HPAPI contract manufacturing facility brings unmatched capacity to the market.
This white paper provides an overview of polymers that can be used in ophthalmic formulations and highlights advantages offered using polyvinyl alcohol (PVA).
This whitepaper provides an overview on the regulatory classification and emerging regulatory challenges for LNP, liposomes, and novel excipients.
The accelerated pathway through the clinic of viral vector-based cell and gene therapies puts pressure on developers to find a skilled partner.
This white paper evaluates the viscosity-reducing capacities of excipients and excipient combinations.
This white paper demonstrates the feasibility of novel virus spiking strategies to meet the needs of continuous processes.
How integrated logistics partners streamline decentralized trials, control costs, and protect ROI.
Released By Yourway Transport, Inc.
AC-201 is being developed to treat multiple immune-mediated inflammatory diseases.
By: Charlie Sternberg
Wendy brings more than 20 years of pharmaceutical quality assurance experience across GLP, GCP and GMP environments.
Parsons will direct compliance strategy, shape operational best practices, enhance regulatory oversight, and mentor future leaders.
Insight on market dynamics driving OSD forms, key development and manufacturing challenges, and the specialized capabilities needed to address them.
By: Ben Locwin
The latest version of its PAS-X Manufacturing Execution System features NextGen cloud and AI support.
CAMCEVI ETM is a long-acting injectable for advanced prostate cancer.
By: Rachel Klemovitch
Will increase global access to AGAMREE for patients with Duchenne muscular dystrophy.
The U.S. Food and Drug Administration (FDA) approved WIDAPLIK on June 6, 2025.
Bayer’s low-dose contrast agent seeks approval for contrast-enhanced MRI of the CNS and other regions for adults and pediatric patients.
Will enhance SGD Pharma’s capabilities and expand its market presence in Europe.
The approval covers the LP.8.1-adapted vaccine, designed to address evolving SARS-CoV-2 sublineages.
Aims to establish a hub for advanced biopharmaceutical production in the MENA region.
For potential new treatment combining BioArctic’s BrainTransporter technology with an undisclosed target in neurodegeneration.
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