mAbxience | Our successful story
Our
successful story
-
2021
• CHMP positive opinion for our MB02 bevacizumab biosimilar.
• Manufacture of the AstraZeneca/Oxford Covid19 Vaccine.
• Bioprocessing Excellence in Southern Europe Award. -
2020
• New state-of-the-art mAbxience biomanufacturing facility opening in Argentina.
• MB02 bevacizumab global regulatory submission.
• Commercial presence via B2B partners in more than 100 markets.
• 3 years of recognized safety standard OHSAS 18001:2007 Certification. -
2019
• New partnerships in EU, Japan, Russia, Canada and other key markets.
• Partnered worlwide with MB02 bevacizumab biosimilar. -
2018
• Alliances with leading pharma companies in EU, USA, and Australia.
• “Business Development of the Year” Award 2018 by GGBA. -
2017
• EMA GMP certification granted to mAbxience Spain.
• First successful Scientific Advices with EMA and FDA.
• Expansion of global access of MB01 rituximab & MB02 bevacizumab. -
2016
• First launch of MB02 bevacizumab (Bevax®, Argentina).
• “Biosimilar Initiative of the Year” Award 2016 by GGBA.
• Global consortium established for the development of MB05 palivizumab*. -
2015
• mAbxience Spain biomanufacturing and R&D center: inauguration.
-
2014
• Acquisition of Genhelix, a Spanish biotech R&D center becoming mAbxience’s scientific and operational hub.
• First launch of MB01 rituximab (Novex®, Argentina). -
2012
• mAbxience Argentina biomanufacturing facility: inauguration.
-
2010
• Established in Europe.
• Acquisition of PharmaADN: mAbxience Argentina R&D platform.
CHMP: The Committee for Medicinal Products for Human Use
GMP: Good Manufacturing Practices
EMA: European Medicines Agency
FDA: US Food Drug Administration
GGBA: Global Generics & Biosimilar Awards
* Programme endorsed by the World Health Organization (WHO) for the treatment of Respiratory Sincitial Virus in pediatric population