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PARIS – October 13, 2021 – Avient Corporation, a premier provider of specialized and sustainable material solutions and services, today announced two additions to its MEVOPUR™ line of medical-grade materials to help producers of pharmaceutical packaging and medical devices more easily reach sustainability goals. Using MEVOPUR medical grade materials can help manufacturers of medical devices and pharmaceutical packaging reduce the risk of regulatory non-compliance. Also being featured at Pharmapack, MEVOPUR foaming agents help manufacturers of pharmaceutical packaging and medical devices add another level of sustainability to their products.

OnColor™ NIR Sortable Colorants for dark packaging recently received APR Meets Preferred Guidance recognition and will be featured in the Avient booth at the Plastics Recycling Conference. OnColor™ NIR Sortable Colorants – enable black and dark packaging to be detected and sorted for recycling and are the most recent innovation to receive APR recognition. In addition, the launch of an exciting new oxygen scavenger technology will be announced on day one of the conference, focused on helping protect beverages in PET packaging.

In fact, ergonomic design of medical devices, diagnostics, equipment and packaging is one of the top trends in healthcare today. Pharmaceutical packaging: Use of soft, non-slip TPEs in caps, closures and other elements can enhance the ability of elderly people to grip, and open and close bottles, jars and other packages.

Companies placing medical devices and packaged pharmaceuticals on the market need their products to comply with healthcare standards, no matter where their products are sold and no matter where they procure their raw materials. 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. Help protect or enhance the performance of polymers used in medical devices, diagnostics and pharmaceutical packaging.

Companies placing medical devices and packaged pharmaceuticals on the market need their products to comply with healthcare standards, no matter where their products are sold and no matter where they procure their raw materials. 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. Help protect or enhance the performance of polymers used in medical devices, diagnostics and pharmaceutical packaging.

For these reasons, medical devices and pharmaceutical packaging products are typically made with standard polymers (e.g., polyolefins, polyesters) and engineering plastics (e.g., polycarbonate, ABS, POM, PBT). However, until recently, these bio-based polymers were used in packaging and consumer plastic products, and most were not assessed for compliance with healthcare regulations. Like all Mevopur products, Mevopur Healthcare Bio-based Polymer Solutions use raw materials pre-tested to ISO 10993-1, USP and , EP 3.1.3 / 3.1.5 (polyolefin packaging materials), USP (polyethylene) and ICH Q3D (elemental impurities).

Thanks to this new additive, converters and brand owners can use higher concentrations of recycled material without compromising packaging aesthetics or performance. at PTI, a package engineering firm, commented that SmartHeat RHC demonstrated "impressive color performance."  Breakthrough technologies that minimize wastewater and improve the recyclability of materials and packaging across a spectrum of end uses.

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