Last May Bioiberica had a non scheduled inspection from the US FDA in its facility in Geneva (Nebraska) where the first steps of heparin sodium production are performed.
Bioiberica is pleased to announce that this three days inspection finished with no deviations.
Once again, Bioiberica was able to demonstrate its extremely high quality level, a key factor to keep its worldwide leading position as heparin sodium manufacturer.
A crucial initiative to prevent shortages of critical medicines in the European Union.
The 28th Symposium on Glycosaminoglycans, an internationally renowned scientific event focusing on glycosaminoglycans, will be sponsored by