FEATURED CONTENT

• Innovation And Flexibility During The COVID-19 Pandemic

  The biopharmaceutical industry has been challenged to discover and develop new diagnostic tests, treatments, and vaccines to help resolve the pandemic. Learn how one CDMO embraces this challenge as they collaborate with customers to develop and manufacture new molecules.

• Improve Biopharma Fermentation With Innovation, Collaboration

  Organizations developing products requiring fermentation often create custom processes from scratch, leaving room for inefficiencies, lost value, and, in the case of significant error, costly time delays.

• Optimizing CDMO Technical Transfer

  Learn how a CDMO helps biopharma organizations predict and mediate technical transfer risks before they become costly, time-consuming problems.

• Grifols Recombinant Protein CDMO

  Grifols Recombinant Protein CDMO, in Emeryville, California, produces recombinant proteins for therapeutics and diagnostics. With services ranging from concept to process development to GMP manufacturing, we look forward to partnering with you to bring your vision to life, together.

• Virtual Panel: Leveraging A Biomanufacturing Legacy To Support New Business

  Grifols Recombinant Protein CDMO has three decades of experience manufacturing recombinant proteins. Recently, the business expanded to apply its experience to producing therapeutic proteins for biopharmaceutical organizations at its new GMP consolidated manufacturing facility (CMF) on its Emeryville, CA, campus. Seven diverse experts discuss how the group’s legacy and recent investments support its future in providing recombinant protein CDMO services.

• 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