Determination of antibiotic impurities in good manufacturing practices-grade cell therapy medicinal products-Reference-Cited by-同舟云学术

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Determination of antibiotic impurities in good manufacturing practices-grade cell therapy medicinal products

Published:2019-10-21 Issue:2 Volume:50 Page:156-163
ISSN:1082-6068
Container-title:Preparative Biochemistry & Biotechnology
language:en
Short-container-title:Preparative Biochemistry & Biotechnology

Author:

Oztel Olga Nehir¹²^ORCID,Korkmaz Seval³,Karaoz Erdal⁴⁵

Affiliation:

1. Liv Hospital – Center for Regenerative Medicine and Stem Cell Manufacturing (LivMedCell), Istanbul, Turkey;

2. Department of Medical Laboratory Techniques, Istinye University, Istanbul, Turkey;

3. YTÜ Technopark İkitelli Campus, Seval Korkmaz Pharmaceutical Ltd., Istanbul, Turkey;

4. Center for Stem Cell Research and Application, Istinye University, Istanbul, Turkey;

5. Histology and Embryology Department, Medical Faculty, Istinye University, Istanbul, Turkey

Publisher

Informa UK Limited

Subject

General Medicine,Biochemistry,Biotechnology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826068.2019.1676780

Reference36 articles.

1. Cell therapy medicinal product regulatory framework in Europe and its application for MSC-based therapy development

2. Cell-based product classification procedure: What can be done differently to improve decisions on borderline products?

3. Klassifizierung von zellbasierten Arzneimitteln und rechtliche Implikationen

4. Immunosuppressive capacity of mesenchymal stem cells correlates with metabolic activity and can be enhanced by valproic acid

5. The Isolation and Production of the Ready-to-Use Product (the Amniotic Stem Cell Culture) in Accordance with Good Manufacturing Practice Regulations

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