It is important that a supplier can offer technical support to help customers test materials, overcome manufacturing issues, and ensure optimum processing parameters are used.   Avient’s Technical Services Team can assist with material testing and processing optimization.  

It is important that a supplier can offer technical support to help customers test materials, overcome manufacturing issues, and ensure optimum processing parameters are used.   Avient’s Technical Services Team can assist with material testing and processing optimization.  

The raw materials are pre-tested to the relevant chapters of ISO 10991, USP 661, USP Class VI, EP 3.1 and to the ICH Q3D guidelines to help manufacturers increase the certainty of regulatory compliance for their devices and packaging. This compliance testing, combined with the support of our healthcare experts, can make transfers of projects involving custom products from one region to another easier and faster.

The raw materials are pre-tested to the relevant chapters of ISO 10991, USP 661, USP Class VI, EP 3.1 and to the ICH Q3D guidelines to help manufacturers increase the certainty of regulatory compliance for their devices and packaging. This compliance testing, combined with the support of our healthcare experts, can make transfers of projects involving custom products from one region to another easier and faster.

Animal Testing Policy We are committed to producing safe products complying with all applicable laws, regulations, and industry standards while avoiding unnecessary animal testing.

In fact, its engineers routinely test and validate a host of new composite applications. Engineers chose this third option because it met all of the technical requirements and had the best combination of properties. For validation, engineers put the braces through an extensive vibration, shake, and road test regime to measure fatigue strength.

Additionally, Avient’s ISO 13485 manufacturing site in Singapore for its Mevopur™ formulations recently achieved ISO/IEC 17025 accreditation for Biological Evaluation of Medical Devices–Part 5: Tests for In-Vitro Cytotoxicity.  Mevopur™ Healthcare Colorants and Functional Additives: formulations pre-tested to support compliance with regulatory requirements, such as USP Class VI, ISO 10993, EP3.1, USP661.1, and ICH Q3D and manufactured across a global network of ISO 13485-certified facilities or under GMP certifications. They are manufactured at an ISO13485-2016-certified site and pre-tested to specific regulatory demands, including USP Class VI and ISO 10993.

Investor Resource Kit

Investor Resource Kit

Investor Resource Kit