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Avient antitrust 2021 update chn a4
https://www.avient.com/sites/default/files/2021-03/avient-antitrust-2021-update-chn-a4.pdf
此会议上发生了什么? 什么是差别定价? 什么是差别定价?
Avient CodeConduct 2023 China
https://www.avient.com/sites/default/files/2023-07/Avient_CodeConduct_2023_China.pdf
我觉 得自己应该报告,但是又有点担心我这样做经理会有 什么反应,她可能会在工作上难为我。 Avient 严禁在 公司的生产经营场所(包括停车场)或在开展公司 业务期间,非法持有、生产、配送、分发、销售或 使用管制物品、毒品或吸毒用具。 我应注意些 什么?
Colorant Chromatics-中文版
https://www.avient.com/sites/default/files/2020-09/ccg-overview-cn.pdf
我们的问题包括: 应用的关键要求是什么? 功能 您的应用要求具有什么功能? 个人客户受限物质清单 药品管理档案 医疗应用文档 食品药品监督管理局(FDA)认证 饮用水认证 Colorant Chromatics 的产品管理用来加强公司的商业行为
Mevopur Standard Colors Product Bulletin-CN3.26-1
https://www.avient.com/sites/default/files/2022-07/Mevopur Standard Colors Product Bulletin-CN.pdf
™ 在三个通过ISO 13485认证的医疗产线生产 全球统一的配方,提供全球一致性和供应链 保障 提供文件化的变更控制 原料指纹图谱和常规批次测试 多种标准颜色缩短产品开发时间 本产品的用户需负责确定埃万特产品是否适合其特定应用。 您有责任进行全面的终端产品性能测试,以确定产 品是否适用于您的应用工艺,同时您还需承担因使用这些资料和/或处理任何产品导致的任何风险和责任。
Avient CodeConduct 2025 ZH CH
https://www.avient.com/sites/default/files/2025-09/Avient_CodeConduct_2025_ZH-CH.pdf
我觉得自己应该报告,但是又有点担心我这 样做经理会有什么反应,她可能会在工作上难为我。 我应注意些什么? 这包括但不限于与以下 事项有关的适用法律法规:贸易禁运、经济制裁、出口管制、反抵 制、关税分类、估价、产品/原产国/地区标记和自由贸易协定。
MEVOPUR Special Effect Colors Application Bulletin_CN
https://www.avient.com/sites/default/files/2022-08/MEVOPUR Special Effect Colors Application Bulletin_CN.pdf
特殊颜料已被成 功应用于个人护理产品和消费品,以增强产品外 观和触感,并增加市场吸引力。 您有责任进行全面的最终产品性能测试, 以确定产品是否适用于您的应用工艺,同时您还需承担因使用这些信息和/或处理任何产品导致的任何风险和责任。 埃万特的产品不为以下目的或用途而设计,也不会宣传或预期用于以下目的或用途: (a) 被美国食品药品监督管理局(FDA)或国际标准化组织(ISO)归类为“
Avient abac china 200721
https://www.avient.com/sites/default/files/2020-07/avient-abac-china-200721.pdf
这些类型的腐败商业活动适用 于我们与之或希望与之开展业务的任何人。 或私营单位员工 目录 2 什么是贿赂? 资料 • 供应商或其他第三方 • 请求向个人或离岸银行账户付款 • 缺乏产品、领域或行业相关经验或缺少合格 的员工 • 反对详细的工作说明书 会计和记录保留要求
MEVOPUR Colors for Ophthalmic Closures Application Bulletin_CN8.18-1
https://www.avient.com/sites/default/files/2021-09/mevopur-colors-for-ophthalmic-closures-application-bulletin-cn.pdf
法规支持 经过预测试的原材料: - ISO 10993-1 - USP 第、章(VI类) - USP (指南),6.2.3 您有责任进行全面的最终产品性能测试, 以确定产品是否适用于您的应用工艺,同时您还需承担因使用这些信息和/或处理任何产品导致的任何风险和责任。 埃万特的产品不为以下目的或用途而设计,也不会宣传或预期用于以下目的或用途: (a) 被美国食品药品监督管理局(FDA)或国际标准化组织(ISO)归类为“
MEVOPUR Bio-based Solutions Application Bulletin_CN5.30-1
https://www.avient.com/sites/default/files/2022-06/MEVOPUR Bio-based Solutions Application Bulletin_CN %281%29.pdf
出设备上进行产品加工的嵌入式解决方案 可以以即用型预着色或添加剂配方的形式提供 • • • • • • 法规支持 原材料根据以下标准检测: - ISO 您有责任进行全面的最终产品性能测试, 以确定产品是否适用于您的应用工艺,同时您还需承担因使用这些信息和/或处理任何产品导致的任何风险和责任。 埃万特的产品不为以下目的或用途而设计,也不会宣传或预期用于以下目的或用途: (a) 被美国食品药品监督管理局(FDA)或国际标准化组织(ISO)归类为“
MEVOPUR Amber for PET Pharma Pkg Application Bulletin_CN5.12-1
https://www.avient.com/sites/default/files/2023-05/Mevopur Amber for PET Pharma Pkg Application Bulletin_CN _2.pdf
Mevopur医疗级琥珀色着色剂和 配方采用经过预测试的原材料,能够确保药品包 装的安全性,同时保护并延长琥珀色PET包装产 品中的药品和营养品的保质期 您有责任进行全面的最终产品性能测试, 以确定产品是否适用于您的应用工艺,同时您还需承担因使用这些信息和/或处理任何产品导致的任何风险和责任。 医疗设备制造商,以及将医疗设备投向市场的人员理应确保医疗设备符合所有适用的法律和法规要求,制造用的所有原材料和部件也必须满足这些要求。

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