PMID: 26319248DOI: 10.1016/j.tibtech.2015.07.002Sep 1, 2015Paper
Closing regulatory gaps: new ground rules for platelet-rich plasma
Trends in Biotechnology
Eduardo AnituaGorka Orive
Abstract
The Spanish Agency of Medicines and Medical Devices (AEMPS) has drawn up a comprehensive report and resolution that regulates for the first time the use of platelet-rich plasma (PRP) as a human-use medicinal product. This regulatory framework offers emerging challenges to adapt the use of PRP to the new requirements of safety and efficacy. The heterogeneity of the different products can hinder their regulation, which today differs substantially in the different worldwide regulatory frameworks.
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Citations
Mar 5, 2016·Platelets·Eduardo AnituaGorka Orive
Mar 2, 2016·Expert Opinion on Biological Therapy·Mikel SanchezSabino Padilla
May 18, 2016·Regenerative Medicine·Eduardo AnituaGorka Orive
Apr 5, 2017·Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics·Ronald Mauricio Sanchez-AvilaLuis Fernández-Vega
Jun 18, 2017·International Ophthalmology·Ronald Mauricio Sanchez-AvilaGorka Orive
Jan 26, 2018·Scientific Reports·Julia EtulainMirta Schattner
Sep 29, 2020·European Journal of Ophthalmology·Marta S FigueroaAndrea Govetto
Mar 1, 2019·Therapeutic Advances in Chronic Disease·Lucía Gato-CalvoElena F Burguera
Apr 9, 2020·Frontiers in Bioengineering and Biotechnology·Paula OnetoJulia Etulain
Jun 29, 2018·BioMed Research International·Tomoyuki Kawase, Kazuhiro Okuda
Sep 19, 2020·Cornea·Eduardo AnituaJesús Merayo-Lloves
Dec 1, 2020·Platelets·Paula Oneto, Julia Etulain
Nov 5, 2020·International Braz J Urol : Official Journal of the Brazilian Society of Urology·Fernando Goulart Fernandes DiasCássio L Z Ricetto
Oct 3, 2020·Heliyon·Wesam El BaklyNesreen Nabil Omar
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