Our ExperTISE
BioCentriq is a global entrepreneurial CDMO with deep expertise in process development and clinical manufacturing. Our multidisciplinary team provides tailored solutions to accelerate the development of cell-based therapies, from early-stage process design to full-scale GMP manufacturing. With a commitment to the highest standards of quality and compliance, BioCentriq helps clients achieve successful clinical outcomes efficiently and effectively.
13+
Cell Types
We’ve worked with a wide variety of modalities, from CAR-T to stem cells, allowing us to navigate the unique challenges of each therapy and push innovation forward.
20+
Lots Released
Delivering consistent results is what we do best. With over 20 clinical lots released, we ensure that every product meets the highest quality standards in the industry.
100+
Years of
Combined
Expertise
Our team brings over a century of combined experience, offering the knowledge and insight needed to guide clients through the complex journey of cell therapy development.
200+
Workforce
Development
Trainees
Our internal teams have trained more than 200 people in GMP manufacturing skills with hands-on programs to include Aseptic Best Practices, Aseptic Gowning and Good Documentation Practice.
Your Cells, Our Mission
Deep Expertise in Process Development, AMD and MSAT
State-of-The-Art, Flexible, and Modern GMP Facilities
Phase-Appropriate Established Quality Systems
LEAPTM Platform for NK, CAR/TCR, T-Cell and Exosome Candidates
Access to Novel Development and Manufacturing Technologies
WHAT WE OFFER
LEAP™ Advanced Therapy Platform
Streamline your therapy’s development with a fully integrated platform that combines manufacturing, analytics, and scale-up. Designed to reduce time to market, our approach ensures your therapy reaches patients efficiently.
Process Analytical Development (PAD)
Optimize every stage of your therapy’s lifecycle with our tailored process and analytical development expertise. From enhancing process efficiency to meeting regulatory standards, we provide the guidance needed to make your therapy market-ready, faster and smarter.
Manufacturing, Science, & Technologies (MSAT)
Drive manufacturing excellence with comprehensive technical support that bridges development and commercial production. Our team focuses on refining your processes, ensuring scalability, and implementing best practices to elevate your manufacturing capabilities.
GMP Clinical Manufacturing
Our expert team and state-of-the-art facilities ensure your therapies are manufactured with precision, compliance, and a commitment to quality, every step of the way.
Workforce Development
Close the skills gap in cell therapy with Biocentriq’s Workforce Development programs, tailored to equip professionals with the latest industry knowledge and practical skills.
Get to know BioCentriq and experience the innovative, collaborative and pragmatic approach we bring to every project.
State-of-the-Art Facilities
BioCentriq owns and operates facilities that are designed exclusively for cell therapy manufacturing. All sites are fully equipped with standard equipment to manufacture autologous and allogeneic therapies using both open and closed processes. We have the quality systems and procedures in place to manufacture and release clinical grade material.
Our facilities provide our manufacturing, process development, MS&T and quality teams with the space and equipment they need to conduct tech transfer and manufacturing, and they contain the supporting infrastructure and labs needed for storage, warehousing, analytical method development, quality control testing, and more.
