ARTICLE SUMMARY:
A sortable and searchable inventory of global medtech regulatory and policy official documents issued in November 2020, including rules, guidance documents, memos, white papers, and more from national authorities, non-governmental groups, and global organizations. Updated November 30.
A final guidance on use of real-world evidence for device submissions in China, an HHS policy statement to prevent “redundant” regulations, and a draft regulation from the Eurasian Economic Union to revise criteria for classification of medical devices are among items recently captured in Pathways’ Document Depot.
