The Regulatory Affairs team at Symbios Orthopédie SA ensures that custom-made orthopaedic implants comply with all relevant global regulations and standards. This involves preparing and submitting documentation for product approvals, maintaining up-to-date knowledge of regulatory requirements, and liaising with regulatory bodies to achieve and retain market access. The team plays a critical role in upholding the company's commitment to safety, quality, and innovation in the medical technology industry.
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