Necm Kimya ISO 13485 (Medical Devices Quality Management System), ISO 9001 quality management system, TC Ministry of Health Biocidal License, CE 93/42 EEC (European Union Medical Device Certificate), BauA (Germany National Occupational Safety and Health Institute approval) ), FDA (United States Department of Health approval), EPA (United States Environmental Protection Agency approval) produces products with certificate.
Necm Kimya offers products in line with international quality standards with its Instrumental Analysis (HPLC, GC/GCMSMS, Spectrophotometer), Chemistry, Microbiology (bactericide-fungus-sporicide-mycobactericide) and R&D Laboratories equipped with advanced technological devices.
The products produced under GMP conditions at Necm Kimya are checked in advanced laboratories and offered for sale.
All of the raw materials used by Necm Kimya in production are purchased from suppliers on the European Union ECHA list. The products it produces are always 1st quality products at world standards.
At Necm Kimya, raw material supply, storage, production stages, post-production storage, shipment conditions and stability tests, and after-sales requests are meticulously evaluated.