Full-scale development projects with a proven track-record in international product launches.
WHY WORK WITH US
Bluepharma offers an integrated approach, providing support on all steps of the product development, from R&D to market.
EU-GMP approved unit, successfully inspected 5 times by US FDA (2009, 2012, 2014, 2016, 2019) and also by MFDS (Republic of Korea), MOH Libya, SFDA (Kingdom of Saudi Arabia), ANVISA (Brazil) and Minpromtorg (Russian Federation). Additionally, the manufacturing sites are registered in Iraq, Jordan, Kurdistan, Taiwan, UAE and Vietnam.
Capability to develop and manufacture high potency products.
Leading contract developer and manufacturer, with an integrated approach.
Long-term partnerships, based on time to market, cost-awareness and a result-driven strategy.
R&D Centers and Manufacturing plant in Portugal.
Differentiated Capabilities
3bn
units per year
on time, in full
right first time
8
packaging lines
lean six sigma
reduced lead time