Matt Taylor is a senior process development associate at KBI Biopharma, where he focuses on the design, optimization, and scale-up of purification processes for biopharmaceutical manufacturing. Matt ...

Additive manufacturing (AM) offers the flexibility to produce unique, innovative designs, inaccessible with conventional production methods, and opportunities for cost-efficient bespoke manufacturing.

Discover how early process design, supported by real-time analytics and advanced process control, can help developers move ...

Aim: To demonstrate the potential of in-line nanoparticle size measurements using the NanoFlowSizer (NFS) as a PAT method. To achieve real-time process control by establishing automated regulation of ...

In drug development many applications are found for lipid-based nanoparticles (Lb-NPs) as successful transporters for poorly water-soluble drugs and oligonucleotides in gene therapy. Major advantages ...

Process validation plays a critical role in the success for a new biopharmaceutical on the path of commercialization, including the crucial process characterization. As a program advances towards ...

The aerospace and defense sector is undergoing rapid material transformation. Additive manufacturing, high-temperature superalloys, advanced aluminum systems, multilayer coatings, and emerging ...

The quality of a drug product is determined by the manufacturing line. Preclinical assessments and clinical trials provide an indication of safety and efficacy, but it is the manufacturing process ...