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MANUFACTURING FACILITY

Sterile and non-sterile production areas and built on 

Üretim Tesisi
+43.000m²

in Ankara, became operational in 2017.

It is designed to have state-of-the-art equipment and built to

conform with Good Manufacturing Practices (cGMP), Good Storage Practices (GSP),

Good Distribution Practices (GDP), Good Laboratory Practices (GLP), and risk-based approaches. 

Manufacturing Capacity

GEN Manufacturing Facility, compliant with advanced technology and high-quality standards,

has European Union Good Manufacturing Practices (EU GMP) approval from Germany Health Authorities. 

Our pharmaceutical products, compliant with high-quality standards, are offered to the markets of Turkey, Russia, Kazakhstan, Azerbaijan, Uzbekistan, the Philippines, and Albania. 
 

Şırınga

40 million Boxes/Year

 The production capacity of liquid

ampoules, liquid vials, lyophilized vials, ready-to-use syringes, and cartridges in the sterile production area 

ilaç

20 Million Boxes/Year

The production capacity of tablets,

film-coated tablets, hard gelatin capsules,

and sachets in the non-sterile production area

The Digital Management Systems We Use in GEN Manufacturing Facility 

SAP

A software system, in which all production, quality, logistics, purchasing, finance, budget, technical maintenance, and human resources operations can be carried out in an integrated, traceable and validated manner.

    EMPOWER 3 FR 5 (Chromatographic Data System)

In our Quality Control and R&D Laboratories, the industry’s most advanced data collection, management, processing, analytical, and reporting capabilities are used to ensure information/data security and product safety at the maximum level and traceability.

Visiopharma Plant Manager

The process is managed with a validated software system that allows printing and tracking data matrix on the products we manufacture and transmitting notifications to our official institutions and licensors.

(Quality Management System)

    QMEX (Quality Management System): All critical quality processes (Modification controls, Deviations, Corrective and Preventive Action (CAPA)) are carried out using a trackable, manageable, traceable and validated software system.

LABX

It is a software system used in our laboratories to ensure workflow efficiency, increase compliance with standards and manage data security.

BMS (Building Management System) 

All our production sites and warehouses; are managed with a system where critical quality parameters such as ventilation, temperature, humidity, and pressure difference can be monitored and recorded 24/7. 

    2D Barcode System

A software system is used to monitor which locations our products are at, such as a pharmacy warehouse, pharmacy, or end-user, with the 2D barcode (matrix code) on them.