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生命科學、生物技術、製藥及醫療器械製造廠商的視覺與標籤系統，全都要面對符合法規的監管要求。這些包括依照 FDA 規定申報，以電子方式提交數位記錄的 FDA 21 CFR Part 11，還有醫療器械標籤與包裝的唯一器械識別碼 (UDI) 要求。美國與歐盟實施這些法規的類似版本。康耐視 Cognex 視覺系統支援符合 21 CFR Part 11 規範，以及 UDI 要求在供應鏈實施的整合標籤管理。