From lab to market: mAbxience’s approach to biopharmaceutical developmentadriana.polo2024-12-02T12:04:35+01:00December 2, 2024|Read More
Biosimilar production: challenges and strategiesadriana.polo2024-11-19T11:06:10+01:00November 19, 2024|Read More
The role of CDMOs in global healthcare advancementsadriana.polo2024-11-20T10:15:33+01:00November 8, 2024|Read More
Single-use technology: how efficient is the present and future of biopharma manufacturing?adriana.polo2024-10-30T16:58:43+01:00October 30, 2024|Read More
Overcoming the complex regulatory challenges in biopharmaceuticalsadriana.polo2024-09-30T18:26:06+02:00September 30, 2024|Read More
Navigating regulatory landscapes in biopharmaceutical manufacturingadriana.polo2024-09-20T10:36:39+02:00September 20, 2024|Read More
GMP certification: ensuring quality in biopharmaceutical productionClara Prieto2024-09-20T09:58:01+02:00August 26, 2024|Read More
Discover the hidden opportunities: real stories of growth at mAbxienceClara Prieto2024-08-14T12:28:54+02:00August 14, 2024|Read More
Mastering biopharma: expert know-how, single-use systems and adaptable manufacturingClara Prieto2024-07-31T16:52:12+02:00July 31, 2024|Read More
From cell to bench and beyond: the manufacturing journey inside mAbxienceClara Prieto2024-07-08T15:31:54+02:00July 8, 2024|Read More