Facilities Designed According to GMP Standards

We have designed our facilities in accordance with ISO 22716:2007 cosmetics GMP standard and have provided each and every detail with respect to the high standards for pharmaceutical raw materials storing. We are still working with care as if it is our first day. We serve with the advantage of having a strong organization and storage infrastructure in product raw material preparation and product packaging.


Select Raw Material Supply Management

As we are aware that raw material supplying is one of the most critical points in magistral drug preparation, we supply pharma grade raw materials directly from the manufacturers whose production facilities comply with GMP standards and ICH Q7 principles.


Analysis and Quality Control

As a part of the importance we place on our work, all raw materials and packaging materials are placed in a quarantine area where temperature and humidity are digitally controlled. There, we perform physical and chemical analysis. We also guarantee the highest goods receiving and production quality by regularly updating the training of our quality control team both inside and outside of our company.

 

Internal and External Laboratory Tests

Product development and quality assurance tests are utilized in own laboratories conforming GMP protocols by Galenik Ecza team.

Production quality is audited and inspected by external reputable laboratories, all accredited by TURKAK (Turkish Accreditation Agency)


"Clean Room" Production System

In our facilities designed for manufacturing at ISO 22716:2007 cosmetics GMP standards, we perform pharmaceutical raw material repackaging and cosmetics products productions in hepa-filtered 100.000 class clean rooms.

 

Continuous Training and Audit

Staying up to date is only possible with training. With this approach, we care for the development of our teams and attend to trainings updated constantly according to the processes. Manufacturing and management systems, teams and facilities are audited by independent auditors twice per year and the complete quality management system is also audited by authorized quality management institutions.