This article provides a comprehensive, up-to-date guide to Good Manufacturing Practice (GMP) standards for producing Mesenchymal Stromal Cell-derived Extracellular Vesicles (MSC-EVs) for clinical applications.
This guide provides a detailed roadmap for researchers and industry professionals aiming to differentiate human embryonic stem cells (hESCs) into neural progenitors under Good Manufacturing Practice (GMP) conditions.
This article provides a comprehensive guide to Good Manufacturing Practice (GMP) processes specifically designed to eliminate tumorigenic risk in pluripotent stem cell (PSC) therapies.
This article provides a comprehensive guide for researchers, scientists, and drug development professionals on establishing robust, Good Manufacturing Practice (GMP)-compliant potency assays for Mesenchymal Stromal/Stem Cells (MSCs).
This comprehensive guide details the critical process of isolating Mesenchymal Stem Cells (MSCs) using GMP-compliant enzymatic digestion.
This definitive guide for researchers, scientists, and drug development professionals explores the critical role of GMP cleanroom classification in cell therapy manufacturing.
This article provides a comprehensive, up-to-date functional comparison of embryonic stem cell (ESC) culture media formulations.
This comprehensive review synthesizes current research on the critical role of FoxO transcription factors in establishing, maintaining, and reactivating genuine quiescence in adult stem cell pools.
This comprehensive guide provides researchers and drug development professionals with an in-depth analysis of flow cytometry-based potency assays for Mesenchymal Stromal/Stem Cells (MSCs).
This comprehensive guide explores feeder-free culture systems for human embryonic stem cells (hESCs), addressing key needs of researchers and drug developers.