Bridging compliance and commercial success in MedTech

At Saolyn we specialise in delivering quality, compliance and innovation to regulated industries — with a particular focus on medical devices and advanced manufacturing. Founded by Ross Prior, we bring over ten years of hands-on industry expertise across engineering, quality assurance, product development and auditing.

We support businesses in navigating complex standards such as ISO 13485, MDSAP, FDA and TGA requirements. From audit readiness and CAPA management to technical documentation and market approvals, we provide practical, results-driven solutions that align with your business goals.

Our mission is to bridge the gap between compliance and commercial success — whether you're launching a new device, expanding into global markets, or streamlining manufacturing. We help you move from checklists to strategic compliance with confidence.