Contract development and manufacturing organization (CDMO) Abzena has announced the formation of a strategic partnership with ...

What seems certain is that space and low-orbit laboratories will become an integral tool for drug innovation within the ...

Biomanufacturing outsourcing growth is slowing, but political uncertainties, tariffs, and labor shortages are reshaping where ...

This case study explores challenges, requirements, and more in adopting next-gen technologies to maintain an edge in process ...

Contract development and manufacturing organization (CDMO) Matica Biotechnology has partnered with Calidi Biotherapeutics to ...

Explore the latest news and expert commentary by Archa Vermani, brought to you by the Contributor of BioProcess International.

Regulatory agencies increasingly are adopting risk-based inspection strategies to ensure that biological products meet stringent safety, efficacy, and quality standards. US Food and Drug ...

Figure 1A: Antibody–drug conjugate (ADC) structure and delivery pathways; linker chemistry determines the mechanism by which cytotoxin release occurs. This schematic shows a monoclonal antibody (MAb) ...

Viral safety is required for biologics manufactured to treat human diseases. Although significant improvements in ensuring viral safety have been made over the past few decades, “zero risk” of viral ...

September 2023 Featured Report ...

The biopharmaceutical industry is at the forefront of technological advancements, with “biopharma 4.0” revolutionizing the way biomanufacturing is conducted (1). The concept combines automation, ...

A number of regulatory guidelines recommend preuse integrity testing of critical sterilizing liquid filters for aseptic processing (1–3). Before sterilization, a preuse test will confirm that a filter ...