VUAB Pharma, a.s.

Reconstruction of premises for production laboratories, supply and installation of technological equipment

2010

Cleanrooms and technologies for the production of API products, corresponding to GMP requirements and cytotoxicity regulations, were implemented. Cleanrooms in purity class 7 – 8 according to ISO 14644–1 („C“ and „D“ according to EU GMP) were built in a total area of about 70 m².