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Sobre mim
Experienced Medical Device Regulatory Consultant with 7+ years of expertise helping manufacturers, importers, and e-commerce sellers navigate global compliance. I specialize in MHRA registration, UKCA certification, FDA registration & listing, and EU MDR documentation (Technical Files, CER, Risk Management). My goal is to ensure your product seamlessly meets international standard requirements without costly delays or rejections. Fast, compliant, and professional service guaranteed.... Saiba mais