*Syringe-Infusion Pump Compatibility Solutions Workshop

The Food and Drug Administration is seeking a third-party organization to develop and facilitate a specialized workshop focused on syringe-infusion pump compatibility solutions. The primary objective of this initiative is to bring together pump and syringe manufacturers to identify critical syringe characteristics that affect pump performance. This collaborative effort aims to establish a technical framework intended to accelerate the creation of a universal compatibility standard, ultimately reducing adverse patient events caused by equipment incompatibility. As a primary outcome of the engagement, the contractor will be responsible for producing a white paper or similar collaborative document. This deliverable will summarize the workshop findings, document areas of industry alignment, and provide strategic recommendations. This document will serve as the foundational evidence and guidance for future development efforts to ensure safer medical device integration.