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A Business Manager at RRxCo, with a background in the Medical Device and IVD space. A strong expertise in generation of business portfolios within MedTech, and project delivery. Our MedTech services include: - EU MDR & IVDR Technical Documentation Authoring - FDA Regulatory submissions; 510(k), De Novo, PMA - CER, PER & PMCF Authoring - Regulatory Strategy - ISO 13485 QMS development and maintenance - Audits Contact Details: Email: [email protected] Phone: +447788260835
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