One partner for the complete process – from design transfer to packaging
Iftest Medical Manufacturing (IMM) helps companies take their products from industrialization through to market-ready production.
By combining design transfer, manufacturing in compliance with FDA regulatory requirements, testing and labeling & packaging, we provide everything needed to manufacture Finished Devices.
The result: safe, traceable products that meet regulatory requirements for international MedTech markets.
Our services
Design Transfer
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.
Manufacturing
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.
Testing
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.
Labeling & Packaging
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.
FAQ
IMM helps MedTech companies turn industrialized designs into market-ready products.
Our service portfolio includes design transfer, manufacturing that complies with FDA regulatory requirements, testing, and labeling and packaging. This gives customers one partner for every essential stage of Finished Device manufacturing.
Bringing all relevant processes together within one organization gives our customers direct communication, clear responsibilities and an integrated quality and compliance strategy.
The result is fewer handovers, lower risk and a faster route to market.
IMM supports MedTech companies in the industrialization and volume production of medical devices for the US market. Documented, audit-ready processes, complete traceability and market-ready Finished Devices put companies in a strong position for a successful market launch.
Contact
We are here for you and happy to answer your questions.
Massimiliano D’Amore
Head of Operations
verkauf@iftest-medical.ch
+41 56 552 55 72
