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Regulatory Strategy Aligned with MDSAP, EU MDR, IVDR, and UK MDR

8 hr
Contact us for quote
US

Service Description

Providing tailored regulatory guidance and quality system support to help medical device Manufacturers comply with evolving global frameworks, such as MDSAP, EU MDR, IVDR, and UK MDR. Whether you're launching a new product or adapting to regulatory changes, I help ensure your compliance strategy is efficient, aligned, and audit-ready.


Contact Details

  • Michigan, USA

    ‪(810) 328-3167

    elizabeth.bernal@medqmscompliancessolutions.com


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