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医療品(医薬品・医療機器・バイオ)該非判定チェックリスト(日本 別表第一 三の項/三の二の項ほか/AG・CWC・BWC・NSG/米EAR・ITAR・2026年版)

医薬品・医療機器・バイオ・製薬化学・核医学を、日本の輸出令別表第一(化学=三の項、生物=三の二の項、核=二の項)・貨物等省令から、オーストラリアグループ/CWC/BWC/NSG、米国のEAR(CCL Category 1・EAR99・744.4キャッチオール)・ITAR(USML Cat XIV)まで記入しながら該非確認できる実務シート。中学生でも分かる超入門つき。個々の病原体を列挙せず公的管理リスト原文を参照する立て付け。e-Gov・AG・OPCW・15 CFRの一次情報に基づく、輸出管理担当者向けのたたき台です(規制は頻繁に改正されるため最終判定は当局の最新公表と貴社の輸出管理責任者を正とします。「非該当(EAR99)=許可不要」ではありません。掲載=規制区分であり企業・国の是非判断ではありません)。

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