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 ...

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 ...

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

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 ...

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 ...

Thought LeadersRobert HighamHead of CfAMUniversity of Bolton/Centre for Advanced Manufacturing Granutools is a Belgian company that specializes in powder flow characterization; the University of ...

Automated characterization is necessary to close the loop between synthesis and discovery of new materials. Through its award-winning faculty, state-of-the-art facilities, and location, the University ...

The courses offered in this catalog are a curated collection of learning materials that provide an overview of Industry 4.0. It is designed to provide resources that businesses can use to understand ...