Compliance Regulations

Streamlining Processes Prior to Trials and Manufacture

Compliance Regulations

Ensuring that healthcare products are user-friendly, compliant with FDA/ISO/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 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 regulatory compliance. Our expertise helps navigate current environmental requirements, such as avoiding hazardous 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 23 countries. 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 target markets with intelligent, digital supply-chain solutions Our flexible approach streamlines the entire product lifecycle, empowering the customer to focus on what matters most to their business — with the peace of mind that Jabil has the rest covered.

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