ARTICLE SUMMARY:
A sortable and searchable inventory of global medtech regulatory and policy official documents issued in December 2020, including rules, guidance documents, memos, white papers, and more from national authorities, non-governmental groups, and global organizations. Updated January 4.
About a dozen new and updated documents issued by the UK Medicines Healthcare products Regulatory Agency in conjunction with the end of the Brexit transition on January 1, three comment solicitations from China’s National Medical Products Administration on planned guidance documents for artificial intelligence medical imaging software, and a product labeling guidance for laparoscopic power morcellators from FDA are among items captured recently by Pathways’ Document Depot.
