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.
Notified body assessment forms under the EU MDR and IVDR, UK NICE technology assessments for sleep apnea and cancer diagnostics, and China NMPA device classification process updates are among items captured recently in Pathways’ Document Depot.
