
Civica is expanding in the greater Richmond-Petersburg region and investing $27.8 million in a new testing facility.

Civica is expanding in the greater Richmond-Petersburg region and investing $27.8 million in a new testing facility.

The White House hopes to expand US modern biotech manufacturing and reduce reliance on foreign sources of bioindustrial materials.

Manufacturing and processing challenges surrounding mRNA can be overcome in order to realize the true potential of a technology 30 years in the making.

Document integrity is critical in the provision of raw materials for cell and gene therapy manufacturing.

For cell and gene therapies to reach their full potential, changes in manufacturing must be explored.

MilliporeSigma’s €130 million (USD$132 million) investment is designed to increase manufacturing capacity of single-use assemblies.

Charles River Laboratories and Cure AP-4 will collaborate on gene therapy manufacturing for AP-4 hereditary spastic paraplegia.

Hovione has expanded its drug product offering with a new manufacturing line dedicated to continuous tableting.

The projected growth in the biosimilars market will require increased bulk mAb manufacturing.

Scaling up chromatography resins requires a thorough understanding of their intended use.

Product safety and security are paramount when it comes to container closures.

More than anything else MonkeyPox and COVID-19 have shown that we are interdependent, no matter what continent you call home.

Forecyte Bio and Cytiva will team up to accelerate the development and manufacturing of cell and gene therapies.

Thermo Fisher Scientific’s new 300,000 ft² facility, located in Plainville, Mass., will specialize in manufacturing viral vectors.

Watson-Marlow and Franz Ziel GmbH have launched a new integrated solution to fast-track cell, gene, and biological therapies.

Grand River Aseptic Manufacturing has completed phase II of its facility expansion with the installation of two new sterile filling lines.

ProBioGen will collobarate with NextPoint Therapeutics to develop and manufacture its lead antibody candidate.

Validair Diamond Scientific has installed a new cleanroom for in-house testing, research, and training.

Guest contributor B.S. Sathya Durga discusses the importance of modernizing India's pharmaceutical manufacturing industry.

The clinical trial research environment has evolved because of specific solutions designed to overcome uncertainty.

The new facility in Albany, Ore., will support biopharmaceutical development and lyophilization services.

Experts divulge where the industry is outsourcing most frequently, when companies should outsource more, and when performing tasks in-house might be best.

The growth in demand of viral-vector-based gene therapies drives continuous efforts to improve viral vector manufacturing.

Automation enables intensification of downstream processes.

Successful scale-up and BLA filings for products manufactured by microbial biomanufacturing require strategic planning.