Eurofins Cdmo

MISSISSAUGA, Ontario--( BUSINESS WIRE )--Eurofins CDMO Alphora Inc. announces the construction of a new GMP Biologics manufacturing facility in Mississauga, Ontario, to manufacture monoclonal Antibodies (mAbs) and protein therapies for clinical and commercial applications. This investment has been complemented with substantial support from the Federal Government of Canada, and a contribution through the Strategic Initiative Fund (SIF), and the facility will bolster Canada's biomanufacturing capabilities and preparedness for future pandemics, while strengthening the biologics ecosystem and employment base in Canada. The 50,000 sq ft biologics manufacturing facility, scheduled for completion in April 2026, will be housed within a new 112,000 sq ft building, constructed on Eurofins CDMO Alphora’s 14-Acre campus in the Sheridan Research Park in Mississauga, Ontario. The facility will be equipped to the 2000L bioreactor scale, employ single-use technology, and be capable of running both fed-batch and perfusion modes. It will provide a fully integrated offering with a state-of-the-art sterile fill line with a capacity of up to 24.9M units annually. This manufacturing facility investment follows the completion of Eurofins CDMO Alphora’s Development & Pilot Scale-up facility, which has been operational since January 2024. This biologics initiative is a pivotal step in Eurofins CDMO Alphora’s strategic vision to provide a suite of integrated solutions, building upon a twenty year history of developing and manufacturing lifesaving and life-improving therapeutics for the Canadian, US and ROW markets. Eurofins CDMO Alphora's expertise in Active Pharmaceutical Ingredients (API) and Highly Potent Active Pharmaceutical Ingredients (HPAPI) uniquely positions it to provide development and manufacturing services for both small and large molecules “under one roof”. This integrated approach facilitates efficient product development and manufacturing, particularly for complex modalities such as Antibody Drug Conjugates (ADCs). Further information: www.eurofins.com/cdmo About Eurofins CDMO Alphora Inc. Eurofins CDMO is a leading global Contract Development and Manufacturing Organization that provides clients with active pharmaceutical ingredients (“API’s”)/drug substance and drug product development for small molecules, biologics and phytocannabinoids via synthetic route. Its service offering encompasses drug substance/API development, solid state research and development, pre-formulation, formulation and development, analytical development, Non-GMP & GMP manufacturing, upstream development, downstream development & ADC Conjugation. Operating with facilities in Europe, North America and India, Eurofins CDMO is accredited through the FDA, EMA, ANSM, ANSES, FAMHP, PMDA, and Health Canada.

MISSISSAUGA, Canada--( BUSINESS WIRE )--Eurofins (Paris:ERF): Eurofins CDMO Alphora Inc. (Eurofins Alphora), a Contract Drug and Manufacturing Organization based in Mississauga, Canada, is excited to announce the successful completion of its pilot-scale biologics development facility. Spanning 3,300 square feet, the facility is dedicated to the development and scaling of monoclonal antibodies (mAbs) and other mammalian-based therapeutic proteins. The facilities’ offerings include upstream and downstream development, process design, analytical development, GMP QC testing, GMP Cell-Based Assays, and scale-up capacity to 200L for pre-clinical and phase I supply. Equipped with cutting-edge technology, the facility can accommodate diverse batch sizes, both fedbatch and perfusion. Leveraging a skilled team of bioprocess scientists and state-of-the-art equipment, such as the Amber 250 and BioProfile FLEX2 Automated Cell Culture Analyzer, Eurofins Alphora prioritizes rapid market entry by implementing efficient, science-based scale-up strategies. The analytical laboratory offers a wide range of analytical testing and bio-assays for both GMP and non-GMP applications, supporting process and drug candidate characterization. This integrated solution enables clients to streamline timelines and reduce development costs in manufacturing biologic drug candidates. Coupled with extensive experience in linker and warhead development through its expertise in active pharmaceutical ingredients (API) and highly potent active pharmaceutical ingredients (HPAPI), Eurofins Alphora’s added biologics capacity supports fully integrated conjugation services for antibody drug conjugate (ADC) candidate development. To learn more, please visit: www.eurofins.com/cdmo About Eurofins CDMO Eurofins Alphora Inc. Eurofins CDMO Alphora Inc. is a leading global Contract Development and Manufacturing Organization that provides clients with active pharmaceutical ingredients (“API’s”) / drug substance and drug product development for small molecules and biologics. Its service offering encompasses drug substance/API development, solid state research and development, pre-formulation, formulation and development, analytical development, Non-GMP & GMP manufacturing and clinical packaging and logistics. Operating with facilities in Europe, North America and India, Eurofins CDMO is accredited through the FDA, EMA, ANSM, ANSES, FAMHP, PMDA, and Health Canada. About Eurofins – the global leader in bio-analysis Eurofins is Testing for Life. With over 61,000 staff across a network of ca. 900 laboratories in 61 countries, Eurofins offers a portfolio of over 200,000 analytical methods. Eurofins Shares are listed on Euronext Paris Stock Exchange (Eurofins Scientific SE (EURONEXT PARIS: ERF)).