Eurofins CDMO Alphora Inc. Announces Construction of GMP Biologics Manufacturing Facility
24 9월 2024 - 10:00PM
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.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240924654060/en/
For further information: Cheryl Young Senior Vice
President, Eurofins CDMO Alphora Inc.
Cheryl.Young@bpt.eurofinsca.com
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