
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。
A closer look at how vision systems help ensure 21 CFR Part 11 compliance related to accessibility, audit trails, and validation.
Explanation of how machine vision systems help identify and track individual medical devices to remain in compliance with governing bodies.
A closer look at how vision systems help ensure 21 CFR Part 11 compliance related to accessibility, audit trails, and validation.
Explanation of how machine vision systems help identify and track individual medical devices to remain in compliance with governing bodies.
取得產品支援與訓練等等
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