ABOUT GRIFOLS RECOMBINANT PROTEIN CDMO SERVICES
Welcome to Grifols. We are an emerging CDMO partner with a focus on producing challenging proteins made in microbial hosts.
Grifols has more than 25 years of experience in recombinant protein technology and we partner with companies interested in developing complex proteins into therapeutics, vaccines, or diagnostics.
We have a cGMP biological manufacturing facility in the San Francisco Bay Area for long-term, high-quality, commercial manufacturing of recombinant biologic drug substance and specializes in recombinant E. coli, yeast and cell culture production.
We are also a provider of Hepatitis C Virus (HCV), Human Immunodeficiency Virus (HIV), and Hepatitis B Virus (HBV) antigens for immunoassay diagnostics. Whether you want antigens from our current menu or custom proteins, our specialists will partner with you to leverage our core development and manufacturing capabilities to provide high-quality, recombinant proteins for your program.
Visit us at the following shows:
- AACC August 5–8, 2019 in Anaheim
- The BioProcessing Summit (Booth 333) August 12-16, 2019 in Boston
- BioProcessing International East (Booth 408) September 9-12, 2019 in Boston.
FEATURED PRODUCTS AND SERVICES
The Benefits of partnering with Grifols
Grifols is ready to partner with you to support development of complex proteins into new therapeutics, diagnostics and vaccines.
Grifols has development and cGMP production capacity for recombinant proteins in yeast.
cGMP production of recombinant proteins made in E. coli is performed in Grifols’ new state-of-the-art facility.
Grifols excels in expressing complex, challenging proteins that don’t fit into a predefined program. Our scientists are creative and innovative applying new techniques to solve problems of yield, protein folding, purity, and more. The best projects are those that have never been done before and have the potential to change the view of medicine or manufacturing.
Grifols has analytical method development and testing to support all stages of product development and manufacturing.
Grifols supplies recombinant Human Immunodeficiency Virus (HIV) antigens including HIV-1, HIV-2 and HIV-1 Type O from the envelope and gag regions. These antigens are currently used in immunoassays that test blood donations worldwide as well as clinical testing of patients.
Grifols supplies recombinant antigens from the Core, NS3, NS4 and NS5 regions of the Hepatitis C Virus (HCV) genome. These antigens are currently used in immunoassays that test >60% of the blood donations worldwide as well as clinical testing of patients.
Grifols supplies recombinant Hepatitis B Virus (HBV) core antigen for immunoassay diagnostics. This antigen is used in immunoassays that test blood donations worldwide as well as clinical testing of patients.
Our HBV antigen is a licensed biologic with the FDA.
CONTACT INFORMATION
Grifols Recombinant Protein CDMO Services
4560 Horton Street
Emeryville, CA 94608
UNITED STATES
Phone: 510-923-6540
Contact: Paul Magreta
FEATURED CONTENT
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![Grifols]( "Virtual Panel: Leveraging A Biomanufacturing Legacy To Support New Business")
Virtual Panel: Leveraging A Biomanufacturing Legacy To Support New BusinessGrifols Recombinant Protein Contract Development and Manufacturing Organization (CDMO) has three decades of experience manufacturing recombinant proteins. Recently, the business expanded its focus to apply its experience to producing therapeutic proteins for biopharmaceutical organizations. Its new GMP consolidated manufacturing facility (CMF) on its Emeryville, California campus supports this expansion.
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![Partners]( "Growing With A Flexible, Collaborative CDMO")
Growing With A Flexible, Collaborative CDMOChoosing a CDMO that is agile, innovative, and exhibits a willingness to invest in new equipment, infrastructure and services will allow the innovator company and the CDMO to grow together.
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![DIA Combination Products Conference]( "Explore Alternative Analytical Methods To Solve Process Challenges")
Explore Alternative Analytical Methods To Solve Process ChallengesSuccessful and rapid analytical method development plays a key role in ensuring the development of robust processes to produce high-quality products.
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![Quality-Lab-Picture]( "Quality Assurance And Your CDMO")
Quality Assurance And Your CDMOThe result of regulatory compliance with quality standards is binary, but the processes employed to get there don't need to be rigid, inefficient, and expensive. Learn how innovation drives efficiencies.
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![Grifols CMF pic]( "Grifols New Manufacturing Facility Provides Contract Development And Manufacturing Solutions For Recombinant Proteins")
Grifols New Manufacturing Facility Provides Contract Development And Manufacturing Solutions For Recombinant ProteinsGrifols' Consolidated Manufacturing Facility (CMF) is a flexible, multiproduct facility with available manufacturing capacity that created an opportunity to leverage their existing technical expertise and commitment to quality to provide contract services to biopharma companies as a recombinant protein CDMO and support the development of innovative therapies. We recently spoke with Paul Magreta at Grifols about their new $80 million manufacturing facility in Emeryville, California, and the CDMO Services they offer.
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![Grifols Building]( "Grifols Achieves Key Milestone With FDA Approval Of The New Consolidated Manufacturing Facility (CMF) For Production Of Recombinant Proteins")
Grifols Achieves Key Milestone With FDA Approval Of The New Consolidated Manufacturing Facility (CMF) For Production Of Recombinant ProteinsEmeryville, CA - Grifols (MCE: GRF, MCE: GRF.P andNASDAQ: GRFS), a global healthcare company with a history of more than 75 years of improving people's health and well-being and a leader in the development of innovative diagnostic solutions, recently received approval from the U.S. Food & Drug Administration to relocate existing immunodiagnostic manufacturing operations to a new Consolidated Manufacturing Facility (CMF) in Emeryville, California
