This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在有意向提交给药政管理当局临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have a...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatoryauthorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have an...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have an...
5、guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。the principles established in this guideline may also be applied to other clinical investigations that may have an ...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have ...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have an...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities.(适用范围) 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that ...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have ...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. 在产生打算提交给管理当局的临床数据时应当遵循本指导原则。 The principles established in this guideline may also be applied to other clinical investigations that may have an...
This guideline should be followed when generating clinical trial data that are intended to be submitted to regulatory authorities. The principles established in this guideline may also be applied to other clinical investigations that may have an impact on the safety and well-being of human subjects...