What Quality Certifications do you maintain? Refer to our website to view certifications: https://www.avient.com/company/policies-and- governance/global-iso-certificate-library Who is Avient’s assessment body/registrar? Annually, with exception of central certificates—at minimum every 3 years.

CERTIFICATE OF INCORPORATION ON CHANGE OF NAME Company Number 3141094 The Registrar of Companies for England and Wales hereby certifies that under the Companies Act 2006: POLYONE CORPORATION UK LIMITED a company incorporated as private limited by shares, havingits registered office situated in England and Wales, has changed its name to: AVIENT MATERIAL SOLUTIONS UK LIMITED Given at Companies House on9th November 2021.

Brown: Please be advised that the office of the Secretary of State has reviewed your pre- clearance request for the Certificate of Amendment for PolyOne Corporation. If you wish to expedite the amendment certificate the fees are listed. NOW, THEREFORE, BE IT RESOLVED, that, effective as of the time and date that the applicable certificate is accepted for filing by the Ohio Secretary of State (the “Effective Time”), the name of the Company shall be changed from “PolyOne Corporation” to “Avient Corporation.”

Progress on TRA Plan ­ Amendments Were any amendments made to the toxic substance reduction plan during the reporting period Description any amendments that were made to the toxic substance reduction plan during the reporting Provide a public summary of the description of any amendments that were made to the toxic substance reduction plan during the reporting Report Submission and Electronic Certification NPRI ­ Electronic Statement of Certification Specify the language of correspondence English Comments (optional)   I hereby certify that I have exercised due diligence to ensure that the submitted information is true and complete.  ON MOE TRA ­ Electronic Certification Statement Annual Report Certification Statement As of 30/04/2018, I, Robert Greenop, certify that I have read the reports on the toxic substance reduction plans for the toxic substances referred to below and am familiar with their contents, and to my knowledge the information contained in the reports is factually accurate and the reports comply with the Toxics Reduction Act, 2009 and Ontario Regulation 455/09 (General) made under that Act. Highest Ranking Employee Robert Greenop Report Submitted by Najat Kamal Website address   I, the highest ranking employee, agree with the certification statement(s) above and acknowledge that by checking the box I am electronically signing the statement(s). 

View PDF The SQS herewith attests that the organisation named below has a management system that meets the requirements of the normative base mentioned. 70 01 _1 /A pr il 20 22 /V er si on 2 .0 Certificate Avient Colorants Spain S.A.

DATA STORAGE UNIT MANUFACTURER D A T A S T O R A G E C A R R I E R • Excellent dimensional stability • Good mechanical properties with excellent wear resistance • Flame retardant requirement – FRv0 compliance • UL certification • Provided a customized formulation to meet application-specific lubricity, physical and thermal requirements • Delivered on short lead times to help customer manage working capital LubriOne™ CY1000-000/5T FR V0 BLK001 Formulation KEY REQUIREMENTS WHY AVIENT?

Certificate No: 33587 Effective Date 25 October 2017 Alex Weisselberg, President

View PDF The SQS herewith attests that the organisation named below has a management system that meets the requirements of the normative base mentioned. 70 01 _1 /A pr il 20 22 /V er si on 2 .0 Certificate Avient Colorants Germany GmbH Hohenrhein 1 56112 Lahnstein Germany Scope Production of Color Concentrates and Compounds Normative base ISO 50001:2018 Energy Management System Reg. no. 46089 Page 1 of 1 Validity 17. 12. 2023  – 16. 12. 2026 Issue 17. 12. 2023  A.Grisard, President SQS F.

2 /Ju n- 20 19 /V er si on 1 .0 Certificate Avient Colorants Singapore Pte Ltd 8 Third Chin Bee Road Jurong Industrial Estate 618684 Singapore Singapore Scope Administration, Site management, Manufacture, Laboratory, Procurement, Maintenance, infrastructure, Warehouse and Transport Normative base EN ISO 13485:2016 Medical devices – Quality Management System Reg. no. 45483 Validity 01. 03. 2022  – 28. 02. 2025 Issue 01. 03. 2022  A.Grisard, President SQS F.

C er ti fi ed M anagement System s by Switzerland Certificate The SQS herewith attests that the organisation named below has a management system that meets the requirements of the normative base mentioned.