Gloria Carmona, MPharm

Gloria Carmona, MPharm

GLORIA CARMONA. MPharm – Head of Quality Assessment and GMP facilities. Qualified Person of the Production and Reprogramming Cell Unit of Seville. Andalusian Network for the Design and Translation of Advanced Therapies (previous Andalusian Initiative for Advanced Therapies).

Gloria has extensive experience in quality management systems and good manufacturing practices applied to advanced therapy medicinal products. She was responsible, between 2007 and 2011, for the design and installation of 10 GMP facilities specialized in Advanced Therapy Medicinal Products, GMP facilities belonging to the Regional Government of Andalusia (Spain) and being coordinated by the Andalusian Network for the Design and Translation of Advanced Therapies. She has been involved so far in the obtaining of the Certificate of GMP Compliance of a Manufacturer or authorization of 6 of these GMP facilities in which she is the coordinator of the activities driven on them. She has carried on the release of more than 900 batches previously produced and certified in the last 10 years at the 6 GMP Andalusian facilities authorized by Spanish Medicine Agency.

Since 2010 she is the Qualified Person of one of these GMP facilities, Production and Reprogramming Cell Unit of Seville, in which they produce cell and tissue engineering products and in the near future also gene therapy products.

She has a wide background in training people up in quality systems and good manufacturing practices, particularly the Master in Manufacturing of Advanced Therapy Medicinal Products in which she is one of the coordinators. She has delivered speeches in diverse national and international conferences in biotechnological field.
Graduated in Pharmacy. Master degree in Pharmaceutical and Parapharmaceutical Industry and Master Degree in Tissue Engineering.