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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.
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