Pfizer has successfully completed its acquisition of Therachon, a privately held clinical-stage biotechnology company.
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Fujifilm Irvine Scientific has announced plans to open a third manufacturing facility in Tilburg, The Netherlands.
Novavax will sell two Maryland-based vaccine development and manufacturing facilities for Catalent’s expanding gene therapy footprint.
The new flow cytometer offers full automation and enhanced software to alleviate bottlenecking.
The company has expanded its high-potency API capability at its Riverview, MI, facility to serve the growing antibody drug conjugates market.
IVERIC bio and Catalent Biologics have entered into a strategic manufacturing agreement for gene therapy product candidates to treat orphan inherited retinal diseases.
The companies have signed a strategic multi-year manufacturing agreement for the future commercial production a late-phase investigational cell therapy.
Catalent will manufacture products for Bristol-Myers Squibb while adding sterile biologics fill/finish and oral solids manufacturing and packaging capacity.
Lyophilization Services of New England acquired a sterile injectables manufacturing facility in León, Spain.
Dassault Systèmes, a provider of virtual universes to imagine sustainable innovations, has signed a definitive agreement to acquire Medidata Solutions in an all-cash transaction.
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The companies will form a biometrics organization focused on delivering analytical solutions for drug development.
The acquisitions, totaling $50 million, are expected expand Aptar Pharma’s service offerings to support complex product development.
The $10-million investment will include a 500-L single-use perfusion bioreactor and seven patented downstream processing units.
Jefferson established the Jefferson Institute for Bioprocessing workforce training institute in collaboration with NIBRT using the GE Healthcare FlexFactory Platform to produce biopharmaceuticals.
Gene therapy development company, bluebird bio, has revealed that the European Commission has granted conditional marketing authorization for Zynteglo.
CDMO iBio introduced cGMP sterile fill/finish services at its facility in Texas.
Shimadzu’s C2MAP-2030 system can improve operational efficiency for optimizing and controlling the cell culturing process.
Agilent’s updated portfolio of products for immunotherapy researchers provides cell-based tools for translational research and development.
Prestige BioPharma has announced that the EMA has accepted its marketing authorization application for HD201 (Tuzune) for review.
MilliporeSigma awarded its Advance Biotech Grant to three US companies that are focused on traumatic brain injury, vaccine development, and chronic pain.
New offering from Catalent targets integrated development and manufacturing of biologic drugs.
By connecting manufacturing processes and logistics technology, GE Healthcare and World Courier look to accelerate the development of advanced therapies.
The companies will develop a new generation of biotherapeutics from cell-line development through to GMP manufacturing.
The expansion will increase the company’s single-use capacity to meet growing demand.
Catalent expands gene therapy capabilities with $1.2-billion acquisition of Paragon Bioservices.
The company announced plans to construct a 1.3 million-ft2 integrated manufacturing center in Chengdu, China.
The acquisition of GlaxoSmithKline’s manufacturing site in Cork, Ireland, will expand Thermo Fisher Scientific’s global footprint for complex API manufacturing.
The partnership will focus on the commercialization of inducible promoters to improve biomanufacturing.
GE Healthcare launches Chronicle GMP-compliant automation software for cell therapy manufacturing.
A UK-based company, Atelerix, has revealed that it has closed a second round of funding worth £700,000 (US$911,000).
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