At Leaman’Ing, respecting your interests is at the heart of our approach. Confidentiality is a fundamental principle we uphold, which is why we have chosen to anonymize testimonials. Each of these reflects the challenges we help solve and the quality of our services, as shared by professionals and organizations who took the time to write them.

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Leaman’Ing was a real partner throughout — clear, adaptable, and focused on results. We turned to Leaman’Ing at a pivotal moment. Our company, active in high-precision surface treatments and laser marking for the watch industry, was preparing to enter the medical device sector as a process subcontractor. While already certified to ISO 9001 and supported by an internal quality team, we needed to raise our quality system to ISO 13485 standards to meet the expectations of new clients and find new prospects.

Leaman’Ing joined our task force and played a central role in helping us close the gaps. Their focused, hands-on approach allowed us to efficiently upgrade our documentation, processes, and validation practices. They quickly understood our constraints and adapted to our reality—without overcomplicating things.

The result: we successfully passed our certification audit in April 2025. Beyond the outcome, what stood out was Leaman’Ing’s ability to make the process clear, manageable, and team-oriented. Their expertise was never just theoretical—they were a real partner throughout.

We’re glad we made this choice and would recommend Leaman’Ing to any company aiming to align with ISO 13485 and take a confident step into the Medtech field.

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« Working with Leaman’Ing has been a positive experience. They supported our Supply Chain and R&D efforts, consistently meeting our needs without backorders in the supply chain and successfully updating our Design History File (DHF) to align with MDR compliance standards.

In addition, Leaman’Ing was instrumental in overseeing our new product design process and provided strong support during various audits and inspections, where they effectively represented our documentation and records without any non-conformities related to their responsibilities.

Leaman’Ing stands out for their pragmatic approach and ability to integrate smoothly with our team and projects. They demonstrate solid leadership and strong soft skills, which make collaboration easy and productive.

I would recommend Leaman’Ing to other organizations seeking support in regulatory and design activities, especially in managing Class 3 Medical Devices. »

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« Leaman’Ing has been instrumental in developing and integrating a Quality System that aligns with our needs and ensures strong project management practices. Since 2020, they provided a consultant who effectively took on a project leader role, fostering collaboration with our internal stakeholders who serve as process owners. Thanks to this structured approach, our Quality System achieved ISO 13485:2016 certification in 2021 for our CDMO scope of Class III HA viscoelastic devices, and we have successfully maintained it each year since then.

Leaman’Ing also managed the relocation of our headquarters in Geneva. In 2023 Leaman’Ing supervised the construction of a 600m² facility and the launch of an ISO-qualified manufacturing environment for sterile injectable Class III devices in Europe. Their team set up all necessary manufacturing and engineering equipment and resources, building a solid foundation for high-quality production.

In addition, Leaman’Ing optimized our supply chain for start and ramp-up of our manufacturing and sales of Class III HA viscoelastic devices, ensuring smoother operations and responsiveness to market demands.

Active in our executive committee, David have also been providing active support in business development and contributed with valuable insights to our executive strategy.

I highly recommend Leaman’Ing to other organizations looking for comprehensive support in quality, manufacturing, and strategic growth »