Article 79: a drug manufacturing enterprise shall establish the written procedures and records of drug return and recall.
第七十九条药品生产企业应建立药品退货和收回的书面程序，并有记录。
Moreover, CGMPs require written procedures for evaluating the quality standards of each drug product at least annually (211.180).
此外，cGMP还要求按照书面程序对每个药品的质量标准每年至少评估一次。
Does your factory have written procedures to make sure that information received from foreign suppliers is reported accurately and timely?
工厂是否有书面程序可用来确认从其他供应商所取得的资讯是正确且准时的？
In some cases, however, the QS regulation does specify the particular type of method to be used, such as written procedures or written instructions.
然而，在有些情况下，质量体系法规确实规定采用某种方法，诸如书面的步骤或书面的指令。
Written procedures should include a list of locations to be sampled.
编写的程序应含有待检测位置清单。
Written procedures may be filed and distributed by automated data processing equipment.
书面步骤也可以通过自动数据处理设备来成文或发布。
Article 38: Written procedures for purchase, storage, dispatching, use, etc. of materials for production shall be established.
第三十八条 药品生产所用物料的购入、储存、发放、使用等应制定管理制度。
Article 38: Written procedures for purchase, storage, dispatching, use, etc. of materials for production shall be established.
第三十八条 药品生产所用物料的购入、储存、发放、使用等应制定管理制度。
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