ISO 13485 certification is a globally recognized standard for quality management systems specifically tailored to the medical device industry. It ensures that organizations involved in the design, production, and distribution of medical devices consistently meet regulatory requirements and deliver safe, high-quality products. Achieving ISO 13485 certification demonstrates a company's commitment to maintaining stringent quality control processes, improving product safety, and complying with industry regulations.
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https://ias-indonesia.org/sertifikasi-13485/