Current Status of PRP Manufacturing Requirements & European Regulatory Frameworks: Practical Tools for the Appropriate Implementation of PRP Therapies in Musculoskeletal Regenerative Medicine

Providing accurate and up-to-date practical tools enabling oversight of platelet-rich plasma (PRP) legislation and of the appropriate standards to be implemented for its manufacture and use in Europe is a demanding task. This is due to rapid medico-technological advancements, slowness and disparity...

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Detalles Bibliográficos
Autores principales: Sebbagh, Patrick, Cannone, Alessandro, Gremion, Gerald, Gremeaux, Vincent, Raffoul, Wassim, Hirt-Burri, Nathalie, Michetti, Murielle, Abdel-Sayed, Philippe, Laurent, Alexis, Wardé, Nathalie, Applegate, Lee Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044789/
https://www.ncbi.nlm.nih.gov/pubmed/36978683
http://dx.doi.org/10.3390/bioengineering10030292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044789/
https://www.ncbi.nlm.nih.gov/pubmed/36978683
http://dx.doi.org/10.3390/bioengineering10030292

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