Ximedica is a leading Outsourced Medical Product Development Accelerator to the Healthcare Industry worldwide. We offer a vertically integrated development process which includes global research capabilities, regulatory and compliance expertise, engineering, global sourcing and introductory manufacturing under a robust Quality Management System.
Healthcare product realization.
We offer a unique capability; a combination of disciplines, process, and deep medical expertise working in conjunction with our clients to bring devices to market in an expedient and accountable manner.
Our people are our greatest asset with disciplines including Research and Strategy, Human Factors Engineering and Industrial Design, six Engineering specialties, Advanced Manufacturing, Quality Assurance and Regulatory. Every project includes a core team comprised of these disciplines with the ability to bring in specialties as needed seamlessly.
Our Quality Management System has been built from the ground up to meet the rigors of the FDA, include the best practices of project management, and innovation techniques while striving to be lean and nimble. Many clients utilize our system as a proxy for their own throughout the development process.
Few companies can match the capabilities of Ximedica. Whether used in part or whole, our integrated capabilities allow clients to bring a medical device to its first clinical trial or launch. Our combined experience has seen hundreds of successful devices enter the marketplace.
Ximedica is ISO 13485:2003 certified by the NSAI (National Standards Authority of Ireland) and FDA registered.