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Experts in Cell Therapy

Advancing Products from Bench to Clinic

Driving Patient Outcomes Through Expertise, Experience, and Commitment.

Our team of experienced engineers, scientists, analysts, and manufacturing staff have hands-on experience in a variety of modalities, platforms, and processes that are essential to the manufacturing of cell therapies.

BioCentriq internal teams work cross-functionally along with collaborating with our clients before, during, and after tech transfer activities for a smooth transition to GMP manufacturing.

Our expertise in process and analytical development, GMP readiness, clinical manufacturing and product release will get you, and your product, from concept to clinic successfully.

BioCentriq augments the client experience by harnessing a hybrid system, where we ensure the client is empowered to be on-site during activities in accordance with our person in plant procedures.

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Workforce Development Trainees

BioCentriq's Expertise Spans Multiple Domains

Our team of experts in R&D, analytical method development, supply chain, manufacturing, project management and quality control and quality assurance have wide-ranging experience and expertise. Our expertise includes but is not limited to the following areas.

Allogeneic Process Optimization and Scale Up

NK (Natural Killer) Cells
MSC (Mesenchymal stem cells)
iPSC (Induced pluripotent stem cells)
Epithelial Cells
Extracellular Vesicles
Cell Encapsulation Technologies

Autologous Process Characterization and Scale Out

CAR-T (Chimeric Antigen Receptor T-cells)
TCR (T-cell Receptor) Engineered Therapies
TILS (Tumor-infiltrating Lymphocytes)
T-reg
MSC (Mesenchymal stem cells)
HSC (Hematopoietic Stem Cells)
Dendritic Cells
Cell Encapsulation Technologies

Analytical Method Development and Qualification

Cell Count & Viability
ELISA
qPCR
ddPCR
Western Blot
Flow Cytometry
Potency/ Cytotoxicity
Nutrient/Metabolite Analysis

We Apply Our Expertise in Several Ways

Scientist in lab operating centrifuge with blue gloves on hands

Clinical Manufacturing

Drug Substance, Drug Product Manufacturing, Fill & Finish, and Release Testing

MSAT

Rapid Transformation of Cell Therapies into GMP Compliance

Process Design & Development

Design and Develop Process Parameters to Optimize Manufacturing

Technology Application

Test the Application and Effectiveness of Emerging and Novel Technologies

Clinical Manufacturing

Manufacture, Harvest, Fill & Finish, and Release Drug Substance and/or Drug Product

MS&T

Apply Continuous Process Improvements & Enabling Technology

Process Design & Development

Design and Develop Process Parameters to Optimize Manufacturing.

Technology Application

Test the Application and Effectiveness of Emerging and Novel Technologies

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The BioCentriq Team

Depending on the approach and scope of your project, your team will include experts from process analytical development, MSAT, manufacturing and quality who have relevant expertise and experience.

In addition, a technical lead will be assigned who is familiar with your underlying technology or platform.

“We've assembled an amazing team with expertise across a wide variety of modalities in cell therapy and they come to us from big pharma, biotechs and our fellow CDMOs.”

David Smith, Ph.D.

VP, Development

“I’ve been working in the biopharmaceutical industry for more than a decade and leverage my educational background in molecular biology and chemistry to take on process development, MSAT, and manufacturing roles in the CGT field. My goal is to apply my expertise to each project to help companies take their therapies from bench to clinic.”