Minimum requirements are adopted from the ISO 9001 standard. Avient requires a Certification of Analysis (COA) and supplier specification documents for every shipment of raw material. Avient categorization for a “supplier” FDA Food & Drug Administration IATF International Automotive Task Force Interested Party Term referenced in ISO 9001.

Certificate No.: CERT-0116814 Original Certification Date: November 24, 2010 File No.: 1616267 Certification Effective Date: April 1, 2021 Issue Date: March 30, 2021 Certificate Expiry Date: March 31, 2024 ________________________________________________________________________________ ISO 9001 Registered by: QMI-SAI Canada Limited (SAI Global), 20 Carlson Court, Suite 200, Toronto, Ontario M9W 7K6 Canada. This registration is subject to the SAI Global Terms and Conditions for Certification. This certificate remains the property of SAI Global and must be returned to them upon request.

Global network of ISO 13485 certified manufacturing sites Browse our library of product data sheets containing technical descriptions and details. See our extensive library of resources about our growing company.

To find more details about our certifications, visit our ISO Certifications Librar y. Avient has 102 global manufacturing facilities. 96% of these sites are certified through independent third parties to management system standards including ISO:14001, ISO:50001, ISO:22000, ISO:45001, ISO:9001, and Responsible Care®. The certification allows all locations on the certification to maintain a Responsible Care® Certification and ISO:14001 certification.

Certificate - ISO 9001 - Avient Corporation - 337726 - 23521672 (1).pdf

Avient’s PCF calculation method follows the ISO 14067:2018 standard and is certified by TÜV Rheinland.   Certified for USP Class VI and ISO 10993, the new Versaflex HC BIO BT218 grade is manufactured in the United States with global commercial availability.   To access Avient's news library online, please visit www.avient.com/news.    

To find more details about our certifications, visit our ISO Certifications Librar y. Avient has 102 global manufacturing facilities. 96% of these sites are certified through independent third parties to management system standards including ISO:14001, ISO:50001, ISO:22000, ISO:45001, ISO:9001, and Responsible Care®. The certification allows all locations on the certification to maintain a Responsible Care® Certification and ISO:14001 certification.

To find more details about our certifications, visit our ISO Certifications Librar y. Avient has 102 global manufacturing facilities. 96% of these sites are certified through independent third parties to management system standards including ISO:14001, ISO:50001, ISO:22000, ISO:45001, ISO:9001, and Responsible Care®. The certification allows all locations on the certification to maintain a Responsible Care® Certification and ISO:14001 certification.

Browse and download our literature to learn more about Avient solutions and services. Browse our library of product data sheets containing technical descriptions and details. See our extensive library of resources about our growing company.

Like other Mevopur formulations, they are produced in dedicated facilities according to ISO 13485-2016 protocols and supported by testing to ISO 10993-1, USP, European Pharmacopeia and ICH Q3D guidelines. About Avient To access Avient’s news library online, please visit www.avient.com/news.