Methods used in the analysis of the pharmaceutical products manufactured by the formulation development department at Turgut Ilaclari A.S. R&D Laboratory fully comply with international pharmacopoeias. All analytical methods are regularly validated by ICH (International Conference on Harmonization) and Ministry of Health criteria.

Turgut Ilaclari A.S. pilot production batches are manufactured by contract companies that hold a GMP (Good Manufacturing Practices) certificate. Raw material and packaging materials are supplied by the subcontractor companies. Physical/chemical property analysis of the finished products and microbiological tests are also performed and certified by subcontractors.

Turgut Ilaclari A.S. R&D Laboratory is an efficient user of the state-of-the-art technologies provided by the IT sector for the storing and monitoring of the data.