Quality Credentials

Cerilliant serves a diverse group of customers and industries who have different quality requirements. Our accreditations provide added confidence to our customers that Cerilliant products are produced and tested to the highest industry standards and are suitable for use in multiple demanding applications and across international borders.

 ISO Guide 34

Accreditation to ISO Guide 34 “General Requirements for the Competence of Reference Material Producers” is designed to ensure competency in the manufacture of reference materials and assurance that international guidelines are followed in the production and assignment of material property values. Accreditation to ISO Guide 34 involves not only technical competence and good quality management practices but adds verification of critical production management specific to reference material producers.

ISO Guide 34 (PDF)


 ISO/IEC 17025

Accreditation to ISO/IEC 17025 “General Requirements for the Competence of Testing and Calibration Laboratories” addresses technical competency of the testing laboratory and specifically, a laboratory’s ability to produce precise and accurate test and calibration data. While designed to be applicable to laboratories running third party samples, accurate test results are critical to the proper characterization of reference materials and, therefore, relevant to reference material producers.

ISO/IEC 17025 (PDF)


 ISO 13485:2003

ISO 13485, “Medical devices - Quality Management Systems – Requirements for Regulatory Purposes”, provides a process oriented approach to developing, implementing, and improving the Quality Management System focusing on ensuring customer and regulatory requirements are met. The ISO 13485 Standard also requires focus on and documentation of risk management activities throughout the product realization process. Certification demonstrates and provides assurance that Cerilliant’s QMS is robust and effective. Cerilliant’s scope of certification is “Design and Manufacture of Analytical Reference Standards, Analytes and Chemicals/Reagents for Use in the Medical Device Industry”.

ISO 13485:2003 (PDF)


 ISO 9001:2008

Cerilliant’s certification to ISO 9001:2008 standard covers all of its operations, including general quality practices; organic synthesis; reference standard manufacturing, testing and certification; and customer and technical service. Certified since 1997.

ISO 9001:2008 (PDF)