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1305 East Houston Street , San Antonio, TX, 78205, US
As the number of new companies in biopharma continues to grow, so does their demand for outsourcing at every level of biopharmaceutical development.
Released By Scorpius BioManufacturing
A global pandemic magnified the need for more biologics manufacturing capacity. Capacity, however, isn’t the whole story.
What is a culture of quality, and how do you know if a biologics CDMO can earnestly make this claim?
Samir Lakhashe, Director, Bioanalytical Sciences, discusses assay categorization, the company's growing toolbox, predictions for the future, and more.
The demand for biologic drugs continues to grow at a steady 12–14% annually.
100 subject matter experts were surveyed from smaller biotech innovators to gain insight into the dynamics and drivers of the current biologics market.
Clinical manufacturing of cGMP-compliant mammalian cell culture processes is a complex and resource-intensive effort that presents several challenges.
Biologics process development is an active undertaking that seeks continuous improvement along the entire length of the drug development timeline.
A look at a CDMO’s value throughout a monoclonal antibody (mAb) therapeutic's lifecycle.
The value biologics CDMOs provide their innovator customers has changed radically in recent years, presenting new questions that must be answered.
The biologics CDMO selected for a given product or program is critical to an innovator’s ability to deliver a drug product safely, on time, and on budget.
When selecting a biologics CDMO partner—whether you need mammalian or microbial capabilities—the decision-making process follows a similar process.
Why Fina Biosolutions partnered with Scorpius Biomanufacturing for cGMP production of Ecocrm® (CRM197)
While crafting a RFP to capture the information innovators need to select a CDMO partner has always been critical; it has grown increasingly complicated.
The partnership includes recovery and downstream process optimization, analytical method implementation and phase-appropriate validation, and more.
Flexible, responsive, customized services for taking a program from R&D into the clinic, using American facilities and American sourced materials and equipment.
Delivering consistent and scalable mammalian-derived products, Scorpius uses its American facilities to advance your drug from R&D to the clinic and beyond.
Scorpius’ team has extensive experience in E. coli microbial biomanufacturing, including hard-to-work-with inclusion bodies.
Utilizing American-made equipment and reagents, Scorpius develops custom assays to profile your molecule and test your clinical trial samples.
Process development & cGMP contract manufacturing for biologics and cell therapies.
A closer look at the chemistry, containment, purification, peptide manufacturing, and sustainability challenges shaping modern API development.
Released By Veranova
New 128,000-sq.-ft. facility in Andover will support the development and commercialization of ADVC001 and its pipeline of Lead-212 targeted alpha therapies.
By: Kristin Brooks
Sponsored By ProBio CDMO
ProChem gains Hanau facilities to expand pharmaceutical manufacturing services.
By: Charlie Sternberg
Biosafety testing facility earns fourth EMA GMP certificate with zero critical findings.
The freezing and thawing platform is designed for maximizing process consistency and product quality for high-value biologics.
By: Patrick Lavery
Sponsored By Adare Pharma Solutions
Forge will provide Skylark with process development, cGMP manufacturing, and analytical development services.
The facility supports a coordinated supply of key RNA manufacturing and IVT workflow materials from early research through commercial production.
Avectas’ automated, integrated, and scalable cell therapy manufacturing platform will be evaluated.
Strengthens its ability to provide a seamless path from DNA to IND submission for its customers.
As development programs become more complex, sponsors increasingly benefit from a coordinated approach that connects clinical strategy, CMC, manufacturing, and supply planning.
Released By Thermo Fisher Scientific Pharma Services
Production is transitioning from Gropello Cairoli, Italy, within the Farmabios business unit.
Advantages of integrated, QbD-guided formulation development services and key strategies for minimizing risk and maximizing success.
By: Eliza Yeung, PhD
Once operational, the facility will be the company's key drug product facility designed to meet the latest and most stringent requirements for international markets.
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