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KİPLAS-Periyod Magazine PharmaVision News

Our General Coordinator’s iSpeak Interview
Career Days in the Pharmaceutical Industry
Explanation Regarding The Eid Al-Fitr Holiday Dates In The PharmaVision Calendar
The Congress on “New Horizons for Pharmaceutical Industry”
European Union (EU) GMP Certificate
Pharmaceutical Production Course Program For Hazardous and Very Hazardous Work Groups

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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.