For over 30 years, Cerilliant has been dedicated to providing Certified Reference Materials (CRMs) for various testing applications, offering over 3000 catalog reference standards as well as OEM and custom products and services. Cerilliant sustains a modern, robust quality system which incorporates cGMP, GLP, and ISO requirements. Quality credentials include accreditations to ISO Guide 34 and ISO/IEC 17025, certifications to ISO 13485 and ISO 9001, and compliance with ISO 17511 and ISO 15194.
Cerilliant serves a diverse group of clients across many industries, ranging from private and government laboratories, hospitals, research institutes, and analytical instrument and medical device manufacturers to pharmaceutical companies and CRO's — organizations that require reference materials of the highest quality, whether they're conducting forensic or clinical toxicology analysis, diagnostic testing, therapeutic drug monitoring, environmental analysis, pharmaceutical research, or developing new testing devices
Products manufactured at Cerilliant are fully documented through the use of batch records to provide traceability of materials used, traceability of equipment utilized, calibration records, and detail of all work performed and staff utilized — all backed by a comprehensive Certificate of Analysis.
