Our facility is fully equipped with the machinery required to manufacture, form and fill solid, semi-solid and liquid dosage forms.
We provide secondary packaging for products whose primary packaging is complete, under GMP conditions and quality assurance oversight. All operations are documented by batch, and products are prepared for dispatch in accordance with the requirements of the Turkish Pharmaceutical Track and Trace System (İTS).
We plan stability studies to help ensure that your products maintain their quality throughout their shelf life. Samples are stored under controlled climatic conditions and analysed at specified time points. All results are documented and reported.
Our studies are conducted in accordance with current ICH guidelines and the requirements of the target market.
We carry out analyses using validated methods, in accordance with current pharmacopoeias, product specifications and applicable GMP requirements. Our modern analytical equipment and experienced team deliver accurate, reliable and traceable results.
We continuously monitor the suitability of the manufacturing environment through environmental and microbiological monitoring programmes in production areas.