European Union (EU) GMP Certificate
After the EU inspection by the French Health Authority, ANSM (Agence Nationale de Securité du Médicament) on 09-12 April 2013, we received our EU GMP Certificate with the cover letter dated July 30th, 2014 from the aforementioned institution.As a consequence and with regards to the qualified person's commitment after the 2013 inspection, the GMP certificate validity has been extended to 12.04.2018 by French Heallth Authority in 14.02.2016.This certification is a concrete indicator of our experience and quality and constitutes an important milestone in the realization of our export-oriented production goals. We are proud and glad to share this achievement with our employees and partners.
At the same time, in addition to our existing EU-GMP certification for our Solid Manufacturing unit, we would like to announce that as a result of the Croatian Health Authority's EU (European Union) audit of our Oral Cephalosporin unit during 08-10 October 2014, we also earned the right to receive EU-GMP certification for these products.
In addition to this, after the inspection by Belarus Health Authority between 27.04.2015-29.04.2015,our GMP compliance has been registered for ”Injectable Cephalosporin" and ”Sterile Liquid” forms .
Also, after the inspection by Ucrain Health Authority between 01.06.2015 - 05.05.2015,we received our Ucrain GMP Certificate for ”Sterile Cephalosporin" and ”Sterile Liquid” forms.
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