The core activity of Leaman'Ing SA is to advise and support companies in the field of medical technology (Medtech). The company's experts offer services in the areas of design, development, manufacturing, quality assurance, certification and supply chain to support companies in the development and marketing of medical products. In particular, the company focuses on compliance with regulatory requirements such as ISO 13485 and MDR.
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Industry:Technical Consulting & Engineering
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Regulatory, quality and engineering consulting for medical devices, with tools and methods tailored to the company, supporting medtech projects in Switzerland, Europe and beyond.
On-Demand Experts
Experts and consultants available on demand, from engineer roles to executive functions and board-level advisory, without a heavy HR process.
Quality & Regulatory Consulting
Design and improvement of the quality system, drafting and implementation, ongoing monitoring, DHF remediation, and support up to regulatory approval.
Medical Device Engineering
Diagnosis of the supply chain and development issues, qualification of medical devices, product scale-up and solutions optimized to reduce risks.
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