Purpose-built ERP software for Medical Device Manufacturers

We Understand the Challenges You're Facing

You're not just making medical products - you're operating under regulatory frameworks that demand complete traceability, controlled processes, and comprehensive documentation. We work with medical device manufacturers every day, so we understand the reality you're facing:

• Regulatory Compliance and Documentation: FDA, CE marking, and other regulatory requirements demand comprehensive documentation. Managing design history files, device history records, and quality documentation is far more manageable with medical device manufacturing ERP software built for regulated environments.
• Full Traceability Requirements: Regulations require the ability to trace products from raw materials through production to end users. Maintaining lot and serial traceability throughout the supply chain is essential.
• Change Control and Validation: Changes to products, processes, or materials require formal validation. Managing change control processes while maintaining production throughput is a key strength of medical device ERP manufacturing software.
• Quality System Integration: Quality management systems require integration with production operations. Capturing quality data, managing non-conformances, and maintaining CAPA records requires structured workflows supported by medical device ERP software.

We've seen it, we've heard it - and we've built Klipboard Manufacturing to help you take control of it.

Klipboard Manufacturing: Built for Medical Device Manufacturing

We don't just tick boxes. We solve the problems medical device manufacturers face every day with medical device ERP software designed to support quality, compliance, and operational control.