Enlil, Inc., (Booth 3908) has launched integrations with Bill.com, PTC Onshape, and Dassault Systèmes SolidWorks. As part of Enlil’s unified platform spanning the entire medical device development lifecycle, these integrations are designed to bring seamless financial and mechanical CAD (mCAD) connectivity into its regulatory-ready environment.
“Enlil unifies MedTech innovation, quality, and compliance in a way that scales with customer needs,” says Nader Fathi, CEO of Enlil. “With Bill.com, Onshape, and SolidWorks integrations, Enlil delivers bi-directional connections that eliminate errors, accelerate time to market, and streamline regulatory readiness — creating a single source of truth unmatched in the industry.”
These integrations underscore Enlil’s commitment to open APIs and purpose-built bi-directional integrations engineered for closed-loop, real-world use cases. The integration with Bill.com enables Enlil users to automate financial workflows as part of a unified lifecycle platform. Benefits include:
- Automated invoice matching against purchase and receiving records.
- Seamless transfer of attachments such as PO PDFs and packing slips into Bill.com.
- Reduced manual effort and errors in financial reconciliation processes.
For product design and engineering, Enlil’s integrations with Onshape and SolidWorks establish the platform as the single source of truth across development. Event-driven CAD-to-Enlil synchronization eliminates manual data re-entry, with the latest design data instantly accessible across engineering, quality, manufacturing, and supply chain functions. Benefits include:
- Automatic propagation of CAD design data into Enlil — including assemblies, drawings, BOMs, and metadata.
- End-to-end traceability from requirements → CAD → BOM → manufacturing → commercial.
- Closed-loop revision and change control, connecting ECOs directly back to design files.
Unlike generic CAD connectors, Enlil builds integration into third-party platforms with MedTech regulatory requirements at the core. By linking CAD design data, BOMs, and engineering change records directly into Enlil, companies can automatically compile the evidence needed for FDA submissions, including Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR). This automation reduces manual effort, mitigates the risk of rejected submissions, and helps companies avoid costly time-to-market delays due to remediation or resubmissions.
