MolMed offers development and production services in two different facilities located in the Milan area.
Both facilities have been designed applying the highest standards in the field of gene and cell therapy in terms of installations, finishes and laboratory equipment according to the GMP guidelines.
- Surface area: about 1.500 mq (16.000 SQF) dedicated to development, testing and production according to cGMP.
- Authorization to produce drugs for clinical and commercial use (2003 and 2015).
- More than 150 GMP batches of viral vectors and over 200 batches of genetically modified cells to support more than 20 clinical trials in Europe and the US
Surface area: about 3.300mq (35.000 SQF) divided in two floors
Designed and built in accordance with the highest quality standards
First Floor: 1.600mq (17.000SQF) dedicated to development, testing and quality control
Second Floor: 1.700mq (18.000SQF) dedicated to the production of viral vectors and Genetically modified cells according to cGMP
10 Grade B suites and 7 Grade C suites
Authorization for the GMP production of viral vectors (on a 48L or 200L scale) and genetically modified cells for clinical trials and market