Automate collection of the production history of medical devices and eliminate paper documents.
Identify problems and non-conformance issues, establish the root cause and create a resolution action plan.
Industry-specific modules to help you achieve compliance with regulatory standards.
Collect and manage electronic signatures to comply with 21 CFR Part 11.
Rely on a secure, centralised document repository to control all documents, including standards.
View custom and standard reporting options, including Recall and Analysis and product/device histories.
Share critical data with customers by enabling them to instantly print detailed tracking reports.
Track and maintain all non-conformances with detailed audit trails for raw materials, work in progress and finished goods.
DELMIAWorks ERP software includes multiple pre-defined BOMs that help you improve the accuracy of your production planning and scheduling.
Our team is 100% dedicated to helping manufacturers of all sizes across multiple industries, including medical devices. We have shop floor experience as production planners and expertise in just-in-time manufacturing processes, so we understand your challenges.
Yes, DELMIAWorks ERP has a specific outsourcing module to manage material movement to subcontractors and receipts following completion of the process. DELMIAWorks also handles the PO and invoicing process.
Yes, the ERP software includes tools that help you meet quality standards demanded by highly regulated industries and individual customers.
