REPROCELL

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Better translating discoveries into therapies. Follow for updates about products, services, and industry news.

Why researchers choose our clinical-grade iPSCs: โ€ข Derived using proprietary, ๐—ณ๐—ผ๐—ผ๐˜๐—ฝ๐—ฟ๐—ถ๐—ป๐˜-๐—ณ๐—ฟ๐—ฒ๐—ฒ ๐—บ๐—ฅ๐—ก๐—” ๐—ฟ๐—ฒ๐—ฝ๐—ฟ๐—ผ๐—ด๐—ฟ๐—ฎ๐—บ๐—บ๐—ถ๐—ป๐—ด technology โ€ข Fully consented donor material with ๐—ด๐—น๐—ผ๐—ฏ๐—ฎ๐—น ๐˜๐—ถ๐˜€๐˜€๐˜‚๐—ฒ ๐˜€๐—ผ๐˜‚๐—ฟ๐—ฐ๐—ถ๐—ป๐—ด โ€ข Comprehensive QC, including ๐—ธ๐—ฎ๐—ฟ๐˜†๐—ผ๐˜๐˜†๐—ฝ๐—ถ๐—ป๐—ด + ๐—ก๐—š๐—ฆ ๐—ผ๐—ป๐—ฐ๐—ผ๐—ด๐—ฒ๐—ป๐—ฒ๐˜๐—ถ๐—ฐ ๐—ฝ๐—ฟ๐—ผ๐—ณ๐—ถ๐—น๐—ถ๐—ป๐—ด โ€ข ๐—™๐——๐—” Drug Master File (๐——๐— ๐—™) available for US generated lines via a LOA โ€ข Starting material for ๐—š๐— ๐—ฃ ๐— ๐—–๐—•๐˜€ & ๐—ช๐—–๐—•๐˜€ for cell therapy use โ€ข Clinical & commercial ๐—น๐—ถ๐—ฐ๐—ฒ๐—ป๐˜€๐—ฒ available
๐—˜๐˜๐—ต๐—ถ๐—ฐ๐—ฎ๐—น ๐—ฅ๐—ฒ๐—ฐ๐—ฟ๐˜‚๐—ถ๐˜๐—บ๐—ฒ๐—ป๐˜ & ๐—š๐—น๐—ผ๐—ฏ๐—ฎ๐—น ๐—ฅ๐—ฒ๐—ด๐˜‚๐—น๐—ฎ๐˜๐—ผ๐—ฟ๐˜† ๐—–๐—ผ๐—บ๐—ฝ๐—น๐—ถ๐—ฎ๐—ป๐—ฐ๐—ฒ: Our donors are recruited in the United States, and the process fully complies with FDA 21 CFR 1271, EMA COMMISSION DIRECTIVE 2006/17/EC, and PMDA MHLW Notification No. 375. All recruitment is conducted under an IRB (Institutional Review Board) approved informed consent protocol. ๐—œ๐—ป๐—ณ๐—ผ๐—ฟ๐—บ๐—ฒ๐—ฑ ๐—–๐—ผ๐—ป๐˜€๐—ฒ๐—ป๐˜ & ๐—œ๐—ป๐—ฑ๐—ฒ๐—ฝ๐—ฒ๐—ป๐—ฑ๐—ฒ๐—ป๐˜ ๐—ข๐˜ƒ๐—ฒ๐—ฟ๐˜€๐—ถ๐—ด๐—ต๐˜: We ensure that all donors provide free and voluntary informed consent, with clear disclosure of potential research, clinical, and commercial applications. The IRB independently reviews our collection protocols to uphold the highest standards of ethics. ๐——๐—ผ๐—ป๐—ผ๐—ฟ ๐—ฃ๐—ฟ๐—ถ๐˜ƒ๐—ฎ๐—ฐ๐˜† & ๐—–๐—ผ๐—ป๐—ณ๐—ถ๐—ฑ๐—ฒ๐—ป๐˜๐—ถ๐—ฎ๐—น๐—ถ๐˜๐˜†: All donors are de-identified and referenced by a unique ID, ensuring confidentiality. This link is securely maintained only at the collection site, following strict IRB guidelines.