oos
美 
英
例句
After a thorough investigation, a firm's QCU might conclude that the initial OOS result did not reflect the true quality of the batch.
經過徹底調查后，公司的質量部門可能認為首次報告的OOS結果不能真實反映該批產品的質量。
Relying on averages of such data can be particularly misleading when some of the results are OOS and others are within specifications.
當出現一些是OOS結果而其它結果的符合規定時，這些數據的平均尤其會造成誤解。
The contest entry that got some of the loudest oos and ahs from the crowd was the Orange Solar Tent from Kaleidoscope.
引發人群最大聲議論的參賽作品是來自萬花筒（Kaleidoscope）的橙色太陽能帳篷。
Such damage would provide evidence to invalidate the OOS test result, and a retest would be indicated.
這樣的破壞能夠證明OOS檢驗結果無效，表明應復驗。
The records and documentation of the manufacturing process should be fully investigated to determine the possible cause of the OOS results.
應該充分調查生產過程的記錄和文件以判斷引起OOS結果的可能原因。
An initial OOS result does not necessarily mean the subject batch fails and must be rejected.
初步的OOS結果并不表示該批次一定是不合格不可以放行的。
OOS test results on these products are considered to be one kind of "information concerning any failure" described in this regulation.
這些產品的OOS檢驗結果被認為是法規所描述的“任何相關失敗信息”的一種。
Handle the out of specification raw material and finished product. Give instruction of action plan of the OOS.
處理原材料和成品的不合格品，給出合理的處理方法。
It should not be assumed that OOS test results are attributable to analytical error without performing and documenting an investigation.
在沒有進行調查和存檔的情況下，不應假定OOS檢驗結果是由于分析錯誤。
The assignment of a cause for OOS results will be greatly facilitated if the retained sample preparations are examined promptly.
如果及時檢測了所保留的樣品制備液，會極大的促進OOS結果原因的確定。
Manage the Change Control, Deviations, OOS investigation as well as the Product Complaints systems.
管理變更控制，進行偏差及實驗結果超標的調查并管理產品投訴系統。
All deviation, investigation, and OOS reports should be reviewed as part of the batch record review before the batch is released.
72在批放行前，所有偏差，調查和不合格報告都應當作為批記錄的一部分進行審核。
Unless the OOS result on the distributed batch is found to be invalid within 3 days, an initial FAR should be submitted.
除非已銷售批次的OOS結果在三個工作日內被確認為無效，否則應提交初始FAR。
QC: complete the correlative mark and written record of OOS results. The related responsibility departments should isolate promptly.
檢驗人員：確實做好不合格品的相關標識和書面記錄，有關責任部門應及時隔離。
The whole unmet demand is lost. The retailers must pay the inventory holding cost and the cost of lost-sales when OOS happens.
認為所有未滿足的需求銷售機會都丟失，零售商既要支付庫存持有費用，又要支付缺貨損失費用。
OOS results are disregarded or negated without a documented investigation.
OOS結果被忽視或沒有記錄的調查否定。
This guidance for industry provides the Agency's current thinking on how to evaluate out-of-specification (OOS) test results.
本指南旨在表達當局對如何評價OOS結果的最新想法。
The RCS must be OOS -MANUAL on both APs before a delete operation is allowed.
在允許進行刪除操作之前，成對的兩個ap上的rcs必須都處于oos-manual。
Despite the deviating trends, no pending potential OOS situation occurs.
盡管背離了趨勢，沒有產生潛在的OOS。
Appropriate testing is needed to ensure that no blending of OOS material is occurring.
合適的測試是為了確保不發生超標批次參與混粉。
When an OOS happens, do you review and check if it would impact other batches?
檢驗數據超標情況發生時，您是否回顧并核實它會不會影響到其它批次？
Report to Supervisor in time when OOT & OOS were found and do further investigation if necessary.
發現OOT和OOS時，及時向領導報告，必要時作進一步的調查。
See the Resources section for more business context surrounding OOS situations.
有關圍繞OOS情況的更多業務上下文信息，請參閱參考資料部分。
Responsible for investigation of OOS results.
負責樣品不合格分析結果的調查。
III. IDENTIFYING AND ASSESSING OOS TEST RESULTS OOS.
檢驗結果的判斷和評估。
IV. INVESTIGATING OOS TEST RESULTS OOS.
檢驗結果的調查。
Do you have an OOS investigation procedure, which follows the requirements of the GMP Guidelines (revised in 2010)?
您是按照藥品GMP（2010年修訂）要求制定的超標檢驗數據調查程序嗎？
OOS out of specification Self-inspection Recall Reprocess Rework Deviation Validation
不符合規定內審產品召回返工再加工偏差
Economical ordering lot model for permit OOS
允許缺貨的經濟定貨批量模型
