《监管活动医学词典》（MedDRA）术语集是在“人用药品技术要求国际协调理事会” （ICH）的主办下编制的国际医学术语集。 本指南对该术语集的编制、范围和结构作了说

The Introductory Guide is intended for use in conjunction with the MedDRA Browsers, available with each MedDRA subscription. Changes which are version specific or changes in …

在 MedDRA 英文版下载文档中，您可通过查阅汇总的《详细报告》（Detail Report）来 查看有关 MedDRA 第 27.0 版考量的所有变更（已批准和未批准）的说明。用户还可在 WebCR上查看自 …

MedDRA is a clinically-validated international medical terminology used by regulatory authorities and the regulated biopharmaceutical industry. The terminology is used through the entire …

MedDRA is a clinically-validated international medical terminology used by regulatory authorities and the regulated biopharmaceutical industry. The terminology is used through the entire …

The Medical Dictionary for Regulatory Activities (MedDRA) Terminology is the international medical terminology developed under the auspices of the International Council for …

• Discuss advanced principles in the MedDRA Term Selection: Points to Conside r (MTS:PTC) document • Discuss MedDRA Concept Descriptions • Show several examples of proper …

《监管活动医学词典》 (MedDRA) 术语集是在“人用药品技术要求国际协调理事会”(ICH) 的主办下编制的国际医学术语集。 本指南对该术语集的编制、范围和结构作了说明。

MedDRA is a clinically-validated international medical terminology used by regulatory authorities and the regulated biopharmaceutical industry. The terminology is used through the entire …

•Present background information about MedDRA and its governance •Review MedDRA’s, scope, structure, and characteristics •Describe the maintenance of MedDRA •Describe MedDRA tools …