医療機器コンプライアンスサポート合同会社

A Regulatory Affairs Certified (RAC) Japanese consultant provides unique and efficient regulatory services online or on site such as SOP reviews or audits in Japanese against applicable FDA regulations including 21 CFR Part 801, 21 CFR Part 803, 21 CFR Part 806, 21 CFR Part 807, 21 CFR Part 812, 21 CFR Part 820, and 21 CFR Part 830.