method validation造句
例句与造句
- research on the method validation of chromatogram fingerprint for qingkailing injection
清开灵指纹图谱验证方法学研究 - methods validation is the process of demonstrating that analytical procedures are suitable for their intended use
分析方法验证是论证某一分析方法适用于其用途的过程。 - the principles of methods validation described in this guidance apply to all types of analytical procedures
本指南中所述的分析方法验证的原则适用于各种类型的分析方法。 - review the validation status of analytical methods validation, process validation and cleaning validation for products
产品的分析方法验证、工艺验证、清洁验证的验证状态的审核。 - the information required for an adequate analytical method validation for either in vitro or in vivo biopharmaceutical studies is discussed in this article
摘要本文将讨论生物药剂学体内、体外试验分析方法论证的必要依据。 - It's difficult to find method validation in a sentence. 用method validation造句挺难的
- this guidance, when finalized, will replace the fda guidance for industry on submitting samples and analytical data for methods validation ( february 1987 )
本指南，一旦定稿，将取代fda于1987年2月份发布的工业指南：分析方法验证所需提交的样品和分析资料。 - the methods validation process for analytical procedures begins with the planned and systematic collection by the applicant of the validation data to support the analytical procedures
分析方法的验证过程是从申请者有计划地系统性收集验证资料以支持分析方法开始的。 - for example, many bioassays are based on animal challenge models, 39 immunogenicity assessments, or other immunoassays that have unique features that should be considered when submitting analytical procedure and methods validation information
比如说，许多生物分析是建立在动物挑战模式，免疫原性评估或其它有着独特特性的免疫分析基础上的，在递交分析方法和分析方法验证资料时需考虑这些独特的性质。 - though more specific analytical issues concerning microbiological assay radioimmunoassay and stereoisomer assay were not examined, this article should provide good guidance to pharmaceutical chemists to properly perform analytical method validation and carry out routine analysis
作者将为从事分析方法认证的工作者提供指南，但对专属分析方法的认证如微生物分析，同位素免疫分析及立体异构体分析未及论述。 - general guidance regarding analytical procedures and methods validation information to be submitted for phase 2 or phase 3 studies will be provided in the fda guidance for industry inds for phase 2 and 3 studies of drugs, including specified therapeutic biotechnology-derived products, chemistry, manufacturing, and controls content and format, when finalized ( draft guidance published april 1999 )
关于在第1阶段研究所需提交的分析方法和方法验证资料方面的指南，发起人可以参考fda的指南：药品（包括结构确定的，有疗效的，生物技术产品）第1阶段研究的ind申请的内容和格式（1995年11月）。 - the most commonly applied assay parameters accuracy, precision, detection limit, specificity, selectivity, calibration linearity or nonlinearity, stability, recovery, reproducibility and repeatability are carefully defined along with some recommendations required for assessing data acceptability arrived at the conference on analytical methods validation
美国分析方法认证会议曾推荐用分析参数（准确度，精密度，检测限度，专属性、选择性、校准线性或非线性、稳定性、回收率、重演性与重覆性）作为判断实验数据的可采纳性。