PathoFinder B.V.
Leah Evers is a seasoned professional in quality assurance and regulatory affairs, currently serving as Quality Assurance/Regulatory Affairs Manager for In Vitro Diagnostics (IVD) at PathoFinder B.V. since March 2022, responsible for maintaining ISO 13485 and IVDR 2017/746 certified QMS. Prior to this role, Leah Evers held various positions, including Quality Assurance Officer and Manager at Medace BV, where the focus was on optimizing quality systems to expedite the market entry of medical devices. Leah Evers also contributed to quality assurance efforts at Chemelot InSciTe and previously worked as a technician involved in the development of PCR kits at PathoFinder B.V. and performed clinical analysis in earlier roles at Orbis medisch en zorgconcern and academic institutions. Leah Evers holds a Bachelor of Applied Science in Life Science from Fontys University of Applied Sciences.
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PathoFinder B.V.
PathoFinder is a molecular diagnostics company, based in Maastricht, The Netherlands, and has developed a proprietary technology platform enabling detection and identification of up 22 pathogens simultaneously. Analysis is performed on a real time PCR instrument. PathoFinder’s focus is on syndromic infectious disease panels and our RespiFinder test is now used in leading hospitals throughout Europe. PathoFinder is ISO13485 certified and all products comply to the CE-IVD guidelines.