谁是 evo820?
FDA监管专家成立了国际咨询公司,以帮助医疗设备制造商保持合规性。
在受人尊敬且知识渊博的行业专家的带领下,evo820 摆脱了FDA 21 CFR 820指南和510(k)提交文件中的头痛和困惑。
Van Bui.
PROJECT MANAGER
Van has 3 years’ experience in the Regulatory Affairs and Quality Assurance field along with 10 years’ experience in the dental industry. She specializes in FDA Quality Systems, client training, customer care, and digital technology, Van works closely with dental laboratories and manufacturers on FDA Matters.