Validation of an automated viable cell counting assay for GMP manufacturing of human induced pluripotent stem cells

Author:

Peli ValeriaORCID,Barilani Mario,Rivera-Ordaz AraceliORCID,Manzini PaoloORCID,Rusconi FrancescoORCID,Lavazza CristianaORCID,Cimoni Silvia,Lazzari LorenzaORCID

Publisher

Elsevier BV

Subject

Biomedical Engineering,Environmental Engineering,Bioengineering,Biotechnology

Reference23 articles.

1. The progression of regenerative medicine and its impact on therapy translation;Jacques;Clin. Transl. Sci.,2020

2. Regenerative medicine: clinical applications and future perspectives;Colombo;J. Microsc. Ultrastruct.,2017

3. Anthony Lodge, G.D. Manufacturing Process Development of ATMPs within a Regulatory Framework for EU Clinical Trial & Marketing Authorisation Applications Available online: https://insights.bio/immuno-oncology-insights/journal/article/467/manufacturing-process-development-of-atmps-within-a-regulatory-framework-for-eu-clinical-trial-marketing-authorisation-applications (accessed on 7 July 2022).

4. Induction of pluripotent stem cells from fibroblast cultures;Takahashi;Nat. Protoc.,2007

5. A manually curated database on clinical studies involving cell products derived from human pluripotent stem cells;Kobold;Stem Cell Rep.,2020

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