Regulatory Compliance

Streamlining Processes Prior to Trials and Manufacture

Ensuring that medical devices and consumer electronics are user-friendly, compliant with FDA/FCC/UL/ETL regulations, and safe for consumers of all ages is essential when bringing virtually any product to market. Yet the pace of the approval process, particularly with medical devices, and increasing numbers of regulatory hurdles impact the industry’s competitive edge both in the United States and overseas. Working with a design and manufacturing company with specialized quality and regulatory knowledge and experience is indispensable to streamlining these processes prior to manufacturing or beginning clinical trials.

Jabil understands the regulations, standards, and best practices that significantly streamline regulatorycompliance. And our expertise helps navigate current environmental requirements, such as avoidinghazardous materials and simplifying end-of-life device disposal.

Jabil Capabilities
Jabil offers end-to-end, comprehensive engineering capabilities with operations at over 90 sites in 23countries. As a single point of accountability, we help:

Innovate and develop designs optimized for performance and manufacturability

Rapidly prototype for accelerated product introductions

  • Manufacture the highest-quality products and components using the latest automation andprocess technologies

  • Stringently validate and test with proprietary, integrated methodologies

  • Ensure that customers build in the right location, source the right materials, and reach targetmarkets with intelligent, digital supply-chain solutions Our flexible approach streamlines the entire product lifecycle, empowering the customer to focus onwhat matters most to their business — with the peace of mind that Jabil has the rest covered.

    For more information on Regulatory Compliance, visit Radius Innovation & Development, the global innovation and product development consultancy of Jabil. 

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