ARTICLE SUMMARY:
A sortable and searchable running inventory of global medtech regulatory and policy official documents, including rules, guidance documents, memos, white papers, and more from national authorities, non-governmental groups, and global organizations.
EU postmarket vigilance guidance for surgical mesh, an update from FDA’s 510(k) Third Party Review Program, and a report on China’s health system reform priorities are among items captured recently in Pathways’ Document Depot.
