片语

OOS Level或断货率

Oos River欧斯河

SENSOR THERMO OOS传感器热缺货

OOS Rooms轻微坏房

OOS listOOS清单

OOS Prometheus普罗米修斯

OOS Clothing售完缺货服装

oos ratio缺货率

OOS Management超标管理

英汉例句

• For this reason, a firm should err on the side of caution and treat the reportable average of these values as an OOS result, even if that average is within specification.

  由于该原因，公司应该倾向于更谨慎，将这些检测值的平均值报告为OOS结果，即使平均值仍符合质量标準。

• The corresponding records of OOS results are preserved by Quality dep. , the storage life of each quality record is requested on quality record list.

  不合格品的相关记录由质量部保存，保存期限见质量记录清单要求。

• There should be no preconceived assumptions as to the cause of the OOS result.

  不应该对OOS结果的原因进行预想的假定。

• QC: complete the correlative mark and written record of OOS results. The related responsibility departments should isolate promptly.

  检验人员：确实做好不合格品的相关标识和书面记录，有关责任部门应及时隔离。

• Appropriate testing is needed to ensure that no blending of OOS material is occurring.

  合适的测试是为了确保不发生超标批次参与混粉。

• Finally, the applicability and validity of the model are testified through its application to OOS development and its effect analysis, and so the theory framework of this thesis is consummated.

  最后，通过该模型在外包软件开发实例中的应用及其效果分析，验证了其适用性和有效性，从而完善了本文提出的理论框架。

• Laboratory managementshould ascertain not only the reliability of the individual value obtained, butalso the significance these OOS results represent to the laboratory qualityassurance program.

  化验室管理不仅应确定所获得的单个值的可靠性，还要确定这些OOS结果代表化验室质量保程序的显着性。

• When evidence of laboratory error remains unclear, a full-scale OOS investigation should be conducted by the manufacturing firm to determine what caused the unexpected results.

  当实验室错误的证据不够确切时，应有生产公司进行全面的OOS调查，以确定是什么引起了意外的结果。

• Does the contract specify the obligations for reporting deviations, OOS and abnormal situations? And which side is responsible for follow-up actions?

  合同中是否明确规定了偏差、超标检验数据和异常情况的报告职责？哪一方负责跟蹤后续措施？

• The AP must be in an OOS state for the initialization to be allowed.

  ap必须处于oos状态才能允许对其进行初始化。

• Invalidation of a discrete test result may be done only upon the observation and documentation of a test event that can reasonably be determined to have caused the OOS result.

  只有在观察到的现象与文件记录表明会导致OOS结果时，才可判定一个与其它数据趋势不符的数据为无效数据。

• To better this customer relationship, this solution reduces OOS situations by tracking in-store shelf availability and reordering stock based on business driven thresholds.

  为了改善这种客户关系，此解决方案跟蹤商店内的货架可用性，并根据业务驱动的阈值重新订购库存，从而减少OOS情况。

• In order to handle OOS results, avoid the misusage of OOS results and insure OOS results without any approval or confirmation should not be accepted, delivered or shifted to the next procedure.

  对已发生的不合格品进行控制，防止误用不合格品，确保不合格品未经批準或确认不得接收、交付或转入下道工序。

• Do you start the OOS investigation immediately after its happening?

  您是在检验数据超标情况发生之后就马上开始调查吗？

• Do you have an OOS investigation procedure, which follows the requirements of the GMP Guidelines (revised in 2010)?

  您是按照药品GMP(2010年修订)要求制定的超标检验数据调查程序吗？

• These appropriate USES of averaging test data should be used during an OOS investigation only if they were used during the original testing that produced the OOS result.

  仅仅当在产生OOS结果的原始检验中使用此平均值时，该平均值才会在OOS调查中被采用。

• Both the initial laboratory assessment and the following OOS investigation should be documented fully.

  最初的实验室评估和以下的OOS调查都应全部存档。

• Indicate the actions you will take if you find that any of the batches you released were OOS for strength, identity, or any other attribute.

  说明如果发现你们所放行的批次的剂量、鑒别和其它属性是OOS，你们将采取的措施。

• In your process development laboratory, our investigator found several unofficial note books recording sample preparation for OOS investigations, route-of-synthesis experiments, and scale-up data.

  在你们的工艺研发实验室，我们的调查人员发现几本非正式记录本记录了OOS调查样品制备、合成路线实验和放大数据。

• When an OOS happens, do you review and check if it would impact other batches?

  检验数据超标情况发生时，您是否回顾并核实它会不会影响到其它批次？

• The records and documentation of the manufacturing process should be fully investigated to determine the possible cause of the OOS results.

  应该充分调查生产过程的记录和文件以判断引起OOS结果的可能原因。

• How does your SOP for OOS define that under which conditions an averaging of results is allowed?

  对于在什么情况下可对(检验)结果取平均值，您的超标检验数据(处理)程序中是怎么规定的？

• OOS test results on these products are considered to be one kind of 「information concerning any failure」 described in this regulation.

  这些产品的OOS检验结果被认为是法规所描述的「任何相关失败信息」的一种。

• It should not be assumed that OOS test results are attributable to analytical error without performing and documenting an investigation.

  在没有进行调查和存档的情况下，不应假定oos检验结果是由于分析错误。

• As with all analytical testing conducted to evaluate the quality of a drug, all records pertaining to the OOS test result should be retained.

  尽管检测是用来评价一种药品的质量，所有与OOS检测结果相关的记录均应封存。

• Report to Supervisor in time when OOT & OOS were found and do further investigation if necessary.

  发现OOT和OOS时，及时向领导报告，必要时作进一步的调查。

• You did not investigate this OOS result or explain why you excluded the failing result from the official record.

  你们没有对此OOS结果进行调查，也没有解释为什么你们在正式记录中排除了该不合格结果。

• Relying on averages of such data can be particularly misleading when some of the results are OOS and others are within specifications.

  当出现一些是OOS结果而其它结果的符合规定时，这些数据的平均尤其会造成误解。