Our team has deep expertise in every aspect of GMP-compliant manufacturing of cell therapy products. We provide a tailored solution, working with your process and analytical panel, or one developed for you by our Process and Analytical Development service. Our comprehensive service offering includes:
Our GMP facilities in Gainesville, Florida, and Research Triangle Park, North Carolina are equipped with the latest technology platforms, staffed by scientists with deep expertise in immunotherapy development and manufacturing.
We have the capacity to handle manufacturing programs ranging from small runs to volume production to support large, multi-site trials.
Kincell Bio is committed to meeting the highest quality standards throughout the development process. Elements of our robust quality assurance program include:
A dedicated Project Manager ensures your manufacturing program stays on track, at every step. Careful planning up-front is focused on ensuring an efficient production process for your product. Our clinical manufacturing experts are available to answer your questions and address any concerns.
Throughout the manufacturing process, we keep you informed with responsive communication.
Featured news
Kincell Bio Inc., a cell therapy contract development and manufacturing organization, today announced the signing of a memorandum of understanding with the Duke University School.
1622 NW 55th Place
Gainesville, FL 32653
20 TW Alexander Dr, Suite 130
RTP, NC 27713
“I think the difference between Kincell and other CDMOs I’ve worked with is the personalized approach to clients. We are working very closely on a one-to-one basis with our clients to ensure that their processes and their aspirations are realized.”
“What excites me every day is the opportunity to deliver better science for our clients and ultimately for the patients we serve.”