{"id":780,"date":"2026-06-08T13:56:04","date_gmt":"2026-06-08T11:56:04","guid":{"rendered":"https:\/\/iftest-medical.ch\/?page_id=780"},"modified":"2026-08-14T10:20:33","modified_gmt":"2026-08-14T08:20:33","slug":"homepage","status":"publish","type":"page","link":"https:\/\/iftest-medical.ch\/en\/","title":{"rendered":"Homepage"},"content":{"rendered":"\n
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Your Swiss specialist partner for FDA-compliant medical device manufacturing<\/h1>\n\n\n\n

Swiss quality for the US market
End-to-end manufacturing
Complete traceability and clear responsibilities<\/p>\n<\/div>\n<\/div><\/div>\n\n\n\n

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Iftest Medical Manufacturing AG (IMM) now adds medical device manufacturing services to its portfolio. We combine our expertise with the engineering capabilities of Iftest AG to provide a seamless service from product engineering and design transfer to the manufacture of Finished Devices for the US market.<\/p>\n\n\n\n

Our services cover design transfer, supplier management, incoming inspection, manufacturing, testing & verification, labeling & packaging, and complete documentation and traceability.<\/p>\n\n\n\n

As one of the few Swiss companies manufacturing Finished Devices in line with the FDA’s regulatory requirements under 21 CFR Part 820, we help MedTech companies transition their products to safe, efficient and consistent volume production for the US market.
Our ISO 13485-certified quality management system and documented, audit-ready manufacturing processes ensure compliance.<\/p>\n<\/div>\n\n\n\n

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Our services<\/h2>\n\n\n\n
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Design Transfer<\/h3>\n\n\n\n

IMM guides MedTech companies through a systematic design transfer process. We ensure that production is based on complete, traceable development data, specifications and quality requirements, and meets all applicable regulatory requirements.
This gives companies a controlled way to industrialize their products safely and efficiently.<\/p>\n\n\n\n

Learn more<\/a><\/p>\n<\/div><\/div>\n\n\n\n

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Manufacturing <\/h3>\n\n\n\n

IMM provides a complete range of manufacturing services for medical devices and Finished Devices. Standardized processes, documented workflows and demanding quality standards support reliable, scalable and auditable manufacturing.
We are responsible for manufacturing in compliance with applicable standards and end-to-end traceability.<\/p>\n\n\n\n

Learn more<\/a><\/p>\n<\/div><\/div>\n\n\n\n

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Testing<\/h3>\n\n\n\n

Our review processes focus on quality and patient safety.
Defined testing and verification procedures ensure that every product reliably and consistently meets the specified requirements.
We document every test result in full, making every result traceable and every process auditable.<\/p>\n\n\n\n

Learn more<\/a><\/p>\n<\/div><\/div>\n\n\n\n

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Labeling & Packaging<\/h3>\n\n\n\n

As a contract manufacturer, IMM is functionally responsible for the finished medical device. That is why we provide labeling, product identification, and final packaging in compliance with regulatory requirements. We deliver each Finished Device complete with Labeling, Packaging, and all required documentation. Market-ready, fully traceable and managed end to end.<\/p>\n\n\n\n

Learn more<\/a><\/p>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n\n

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Industries<\/h2>\n\n\n\n

Our customers develop innovative products for regulated markets. IMM helps companies in medical technology, diagnostics, laboratory automation and related high-tech fields industrialize their products and move them into volume production for the US market.<\/p>\n\n\n\n

Learn more<\/strong><\/a><\/p>\n<\/div>\n\n\n\n

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Quality & Compliance<\/h2>\n\n\n\n
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ISO 13485:2016<\/a><\/strong><\/p>\n<\/div>\n\n\n\n

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FDA registration (pending)<\/strong><\/p>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n

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FAQ \u2013 frequently asked questions<\/h2>\n\n\n\n
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