Combining OnColor Bio with bio-based polymers helps to reduce the risk and cost of post-process testing. OnColor Bio concentrates have received OK compost HOME certification from TÜV AUSTRIA, a leading independent testing firm. Using these concentrates in bio-degradable packaging can help avoid the significant costs and time required to test products for at-home compostability.

Customizable colors and pre-tested raw materials to help simplify production and minimize risk, and impact-resistant thermoplastics for extended product life. Customizable colors and pre-tested raw materials to help simplify production and minimize risk, and impact-resistant thermoplastics for extended product life. Formulated with pre-tested raw materials, this range of additives helps enhance the performance and functionality of plastics used in medical devices and pharmaceutical packaging and mitigate the risk of non-compliance.

These unique MEVOPUR™ concentrates use pre-tested ingredients and prescribed manufacturing practices to help customers achieve compliance with pharmaceutical packaging regulations through 2025 and beyond.  They are formulated without animal-derived substances and phthalates, and have been pre-tested for compliance with: •    ISO 10993-1 and USP parts , (including class VI) •    European Pharmacopoeia, monograph 3.1.15 •    USP and •    elemental analysis, as per ICH Q3D In this case, the newest amber masterbatches comply not only with the current USP 661 standard, which governs plastic materials used in pharmaceutical packaging, but they have also been tested for compliance to USP regulations that won’t become effective until December 2025.

SYNTHESIS TEST DATA MIX 12 SYNTHESIS TEST DATA MIX 10 SYNTHESIS TEST DATA MIX 11

TEST FORMULA #3 TEST FORMULA #4 TEST FORMULA #5

9874 LT ASH GREY 3325MT TESTING ONLY 313N DK TITANIUM 6500 TESTING ONLY 313N DK TITANIUM 6500 TESTING ONLY

Tests show a light fastness of 7 on the blue scale and 4 to 5 on the grey scale (FAKRA) and rubbing and washing fastnesses of 4 to 5. Fastness tested Tests carried out by external laboratory

Examine the technical details of our research study to test against microbial attack, including the efficacy of GLS™ TPES with antimicrobial additives Provided easy injection molding process and pass durability test with good wear resistance

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.

This is particularly evident in the expanding market of point-of-care testing (POCT) where diagnostic devices such as blood monitoring systems and test kits for infectious diseases and viruses (flu, COVID-19, HIV) are becoming more accessible to the public. Color and special effect masterbatches pre-tested to ISO, US Pharmacopeia, European Pharmacopoeia, and ICH Q3D protocols for differentiation and patient adherence support Color and additive solutions based on biopolymers pre-tested to ISO, US Pharmacopeia, European Pharmacopeia, and ICH Q3D protocols to reduce product carbon footprint