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.
Virtual Panel: Leveraging A Biomanufacturing Legacy To Support New Business
Grifols 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.
Growing With A Flexible, Collaborative CDMO
Choosing 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.
Explore Alternative Analytical Methods To Solve Process Challenges
Successful and rapid analytical method development plays a key role in ensuring the development of robust processes to produce high-quality products.
Quality Assurance And Your CDMO
The 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.
Grifols New Manufacturing Facility Provides Contract Development And Manufacturing Solutions For Recombinant Proteins
Grifols' 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.
Grifols Achieves Key Milestone With FDA Approval Of The New Consolidated Manufacturing Facility (CMF) For Production Of Recombinant Proteins
Emeryville, 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