Purpose-built Medical Device ERP Software for Africa

We Understand the Challenges You're Facing

You’re not just producing medical devices; you’re operating within regulatory frameworks that demand complete traceability, controlled change processes, and comprehensive documentation. We work with medical device manufacturers supplying local healthcare providers and export markets, so we understand the challenges you face:

• Regulatory Compliance and Documentation: Regulatory frameworks such as SAHPRA requirements, ISO 13485, and customer-specific quality expectations demand structured documentation. Managing design history files, device records, and quality documentation is significantly more controlled with ERP software built for regulated medical environments.

• Full Traceability Requirements: Medical device regulations require traceability from raw materials through production to distribution. Maintaining accurate lot and serial tracking across the supply chain is essential for patient safety and recall readiness.

• Change Control and Validation: Changes to products, processes, or materials require formal review and validation. Managing controlled change processes while maintaining production throughput is critical to compliance and operational stability.

• Quality System Integration: Quality management systems must be tightly integrated with production. Capturing quality data, managing deviations, and maintaining CAPA records requires structured, system-driven workflows. 

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. Klipboard addresses the day-to-day challenges medical device manufacturers face, with ERP tools designed to support quality, compliance, and operational control.