ILKO's main aim is to ensure the delivery of our products to patients in the same standards and most reliable manner with ah quality and process-oriented production approach.
is innovative and leader in human pharmaceutical production and medical device industry, developing the product range by following the innovations in the healthcare industry,
maximizes customer satisfaction without compromising from quality,
conducts in conformity with the laws, regulations, national and international standards (Medical Device Regulations, ISO 13485 Quality Management System, Good Manufacturing Practices (GMP)),
guarantees the marketed products to have the technical specifications foreseen in the standards of the product,
maximizes product quality by ensuring effective application of the quality system at all stages of production,
monitors the quality processes periodically, analyzes the results, makes continuous improvements with corrective and preventive activities,
Ensures participation of every employee within the organization; plans and realizes all training activities required to leverage quality awareness, thus gathers them around the same mission, vision and strategy and creates a shared corporate culture,
ensures effective operation of the quality system to cover the customer's requirements and legal requirements,
provides resources for the improvement activities through continuous revision of the effectiveness of the existing quality system and the quality objectives created in accordance with the quality policy,
manufactures its products with a proactive approach against risks,
implements an effective Quality Assurance System beginning from the quality controls before using the beginning materials at Quality Control Laboratories, and continuing with semi-finished product, in-process controls at various steps of production, finished product quality controls and effective environmental controls.
It ensures that all raw materials, packaging materials and finished products entering the processes and formed as a result of the processes are stored in appropriate conditions, customs are cleared in accordance with the relevant process steps, and their foreign trade is carried out in accordance with the principles of authorized obligations.