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filler@godaddy.com
Want to take your invention to the clinic?
Use our expertise to translate your research findings to clinically suitable cell and gene therapy products via identifying materials of high grade, disposables and equipment of closed systems, and GMP-compliant process
Interested in a new process?
We collaborate with the cell and gene therapy technology originator and share skills, knowledge, technologies, and methods and make it your own
Need to determine the feasibility of a new process?
We help you do this by working with you to design experiment, identify materials, optimize conditions, collect and analyze data
Want to qualify your test assay?
We help you identify, develop, validate, and optimize new assays to ensure quality of cell therapy processes and products
Process development is easier when you consider the end points. We help you design a process that meets quality and regulatory requirements, and ensure scalability and efficiency of the process while observing the required time frame
Start early and save your efforts. To ensure your process development meets the relevant institutional and regulatory cell and gene therapy standards, we help you develop the validation protocol, review the data and the final report
You have been successful in your early studies and it is time to scale up? Identify the requirement to produce larger doses of your cell and gene therapy product. This include increasing the production capacity in terms of personnel, efficient use of facility, storage, release and distribution
Are you ready for GMP production?
Let us help you identify GMP requirement, develop readiness checklists, and ensure readiness for GMP production of your cell and gene therapy product
POTENTCELLS
Saudi Arabia
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