Limitação de Responsabilidade. Termos de ajustes. Escassez de produto.

A validade deste certificado é baseada em auditorias periódicas do sistema de gestão definido pelo escopo acima e está condicionada à notificação por escrito ao ABS Quality Evaluations, Inc. de mudanças significativas no sistema de gestão ou seus componentes. Francisco Nakasato, 1700 Bairro São Roque das Chaves Itupeva, SP 13295-000 Brasil ISO 9001:2015 O Sistema de Gestão da Qualidade é aplicável a: Certificado No: 49862 Data de Expiração Anterior: 09 Abril 2020 Data de Aprovação Original: 16 Abril 2014 Data de Certificação: 13 Abril 2020 Data Efetiva: 06 Abril 2023 Data de Expiração: 09 Abril 2026 Data de Emissão: 06 Abril 2023 Dominic Townsend, Presidente DEVELOPMENT, PRODUCTION, SALES AND TECHNICAL ASSISTANCE OF LIQUID COLORANTS, COLORS CONCENTRATES AND ADDITIVES FOR THE PLASTICS, FIBERS AND RUBBER MARKET IN GENERAL DESENVOLVIMENTO, PRODUÇÃO, VENDAS E ASSISTÊNCIA TÉCNICA DE COLORANTES LÍQUIDOS, CONCENTRADOS DE CORES E ADITIVOS PARA O MERCADO DE PLÁSTICOS, FIBRAS E BORRACHAS EM GERAL. Certificado de Conformidade

KEY CHARACTERISTICS • Available for polyethylene, polypropylene, ABS, polycarbonate and styrenics • Bio-content of resin carrier varies from 70% to 100% depending on polymer—calculated to ASTM D6866 standard • Manufactured at four ISO 13485 certified sites, providing global consistency and security of supply • Documented change control beyond CAS number, reducing risk of change • Drop-in solutions that can be processed like fossil-based grades on common injection molding and extrusion machines • Can be provided as ready-to-use pre-colored or additive formulation REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 - USP and (incl. class VI) - European Pharmacopeia, monograph 3.1.3/ 3.1.5 (polyolefin packaging materials) - USP (polyethylene) - Elemental impurities as per ICH Q3D • Registered Drug Master File (Type III) and/or Device Master File • Food contact according to US FDA and APPLICATION BULLETIN Sustainability Spotlight Bio-polymers Healthcare use limitations apply—see below.

REGULATORY SUPPORT • Drug delivery devices • Pharmaceutical packaging • Medical equipment KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified sites, providing global consistency and increased security of supply • Documented change control beyond CAS number level, reducing the risk of change • Allows crystallization in semi-crystalline polymers to begin faster and complete earlier REGULATORY SUPPORT • Raw materials tested to: - ISO 10993-1 and USP biological evaluation - European Pharmacopeia 3.1.3/3.1.5 (polyolefin) - USP (polyethylene) - ICH Q3D elemental impurities • Registered Drug Master File (Type III) and/or Device Master File • Food contact established with FDA/EU* APPLICATION BULLETIN * FDA/EU compliance information available upon request Healthcare use limitations apply—see below.

KEY CHARACTERISTICS • Manufactured at four ISO 13485 certified sites, providing global consistency and increased security of supply • Documented change control beyond CAS number level, reducing risk of change • Non-phthalate and formulated without animal-derived substances • Different tones of amber available on request —more or less red or yellow and/or lighter or darker • Also available in liquid form REGULATORY SUPPORT • Pre-tested raw materials: - ISO 10993-1 and USP parts (Class VI) - European Pharmacopeia, monograph 3.1.15, USP and elemental analysis as per ICH Q3D - USP criteria appearance of solution, color • Registered Drug Master File (Type III) by the FDA • Food contact compliance established with FDA/EU* • YBB00102002-2015 (oral liquid pharmaceutical PET bottles) compliance support APPLICATION BULLETIN * FDA/EU compliance information available upon request Healthcare use limitations apply—see below.

FABRICANTE DE EMBALAGENS FARMACÊUTICAS G A R R A F A S Â M B A R • Garantir a conscientização sobre os padrões e requisitos de conformidade aplicáveis • Fornecer opções de matéria-prima que estejam alinhadas com os padrões brasileiros de embalagens farmacêuticas • Aderir às Boas Práticas de Fabricação (BPF) • Colaborou em toda a cadeia de suprimentos para garantir que as necessidades regulatórias de matéria-prima fossem atendidas • Avaliação da conformidade das matérias- primas com os padrões brasileiros de embalagens farmacêuticas • Material produzido sob os requisitos de BPF Hiformer Liquid Masterbatches PRINCIPAIS REQUISITOS POR QUE A AVIENT? https://pt.avient.com/products/polymer-colorants/liquid-color-concentrates/hiformer-liquid-masterbatches Slide 1: Fabricante de embalagens farmacêuticas

Spolupráce se zástupci, distributory a dalšími třetími stranami Společnost Avient může čas od času využít zástupce, distributora, poradce nebo jiného prostředníka k podpoře svých obchodních aktivit nebo může spolupracovat s obchodními partnery ve společném podniku nebo v jiné obchodní struktuře. Francisco Nakasato, 1700 13295-000 Itrevea Sao Paulo, Brazílie Telefonní číslo: +55 11 4593 9200 Evropa Regionální centrála Pommerloch, Lucembursko 19 Route de Bastogne Pommerloch, Lucembursko, L-9638 Telefonní číslo: +352 269 050 35 Fax: +352 269 050 45 www.avient.com https://www.avient.com

Copia Escritura - ACTA SANTIAGO Certifico que el presente documento electrónico es copia fiel e íntegra de ACTA otorgado el 31 de Mayo de 2021 reproducido en las siguientes páginas. Repertorio Nro: 8412 - 2021.- SANTIAGO, 31 de Mayo de 2021.- Emito el presente documento con firma electrónica avanzada (ley No19.799, de 2002), conforme al procedimiento establecido por Auto Acordado de 13/10/2006 de la Excma.

La mise en œuvre de ces normes en termes de performance des fournisseurs est importante pour nous, et nous attendons de nos fournisseurs et partenaires commerciaux qu’ils communiquent ces attentes tout au long de leur chaîne d’approvisionnement en adoptant des systèmes de gestion, des politiques, des procédures et une formation efficaces pour respecter les normes et les attentes énoncées dans ce code de conduite des fournisseurs au sein de leurs opérations commerciales. S’abstenir d’offrir de l’argent, des prêts, des crédits, des remises préjudiciables, des cadeaux, des produits ou des services à des collaborateurs d’Avient pour leur usage ou leur avantage personnel. Éviter les conflits d’intérêts qui impliquent des relations commerciales avec des membres de la famille et des amis personnels proches chez Avient.

Lo ss ta ng en t NEW TECHNOLOGIES REQUIRE NEW MATERIALS The rapid technology development requires new frequency ranges and bandwidths.