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• Declarations based on pre-testing of the ingredients we use to standards typically required for medical and diagnostic devices (biological evaluations ISO10993, USP , for class VI devices); and for pharmaceutical packaging and drug-contacting materials (biological evaluation USP, EP chapter and requirements USP and ICHQ3D extractable metals).
• Letter of Authority (LoA) for our Drug Master File (DMF) and Device Master File (MAF).
• Disclosure of ingredients for purpose of regulatory filings (under specific confidentiality agreements).
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Contact our team of experts if you’d like assistance evaluating the pros and cons of sustainable or conventional options.
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Food contact-approved special effects
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Detailed regulatory information is available from your Avient contact.
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Contact our experienced team to collaborate globally on the design of your lightweight next-gen wearable devices to deliver brilliant aesthetics, haptics, and performance.
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Contact us to discuss the value Cesa Percept Authentication Technologies can bring to your organization.
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If you’d like assistance evaluating any of these factors, contact us.
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Food contact approved formulations are available