The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Senate passes counterfeit device destruction bill; MHRA posts device compliance dates for Brexit.

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Advanced Bionics, Advanced Medtech, Laboratory Corporation of America, Oxford Immunotec Global, Recor Medical, Virocule.

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Anade, Applied Biosystems, Aural Analytics, Corvion, Cytosorbents, Diagnosticos da America, Establishment Labs Holdings, Everheart Systems, First Nation Group, Fresenius, Globus Medical, Haliodx, Irras, Lucence, Microport Cardio Rhythm Management, Nightware, Novocure, Rewalk Robotics, Sectra, Stata Oncology, Thermo Fisher Scientific, Tridiuum, Twist Bioscience, Viveve Medical, Vivos.

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Adial, Alligator, Ampio, Arcus, Aytu, Axcelead, Biomx, Caamtech, Evommune, Fusion Antibodies, Heat, Hemoshear, Kazia, Monopar, Neos, NGM, Oncoceutics, Purnovate, Salarius, Synedgen, Vaccibody, Wuxi, Takeda.

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abbvie, Abivax, Advaccine, Apellis, Arbutus, Bellicum, Biontech, Clene, EOC, Fusion, Gensight, Geron, Immutep, Inovio, Kintor, Moderna, Obseva, Pfizer, Pharming, Puretech, Regenxbio, Savara, Sobi, Spero, Stalicla, Sunovion, TG, Tracon, Ultimovacs.

The U.S. FDA authorized Burlington, N.C.-based Laboratory Corporation of America Holdings’ (Labcorp’s) Pixel COVID-19 test home collection kit for use by any individual 18 years and older without a prescription.

The latest U.S. FDA town hall for diagnostics included the usual technical questions about test validation, but there are some frustrations among test developers regarding turn-around times for emergency use authorizations (EUAs). Nonetheless, Tim Stenzel, director of the Office of In Vitro Diagnostics and Radiological Health (OIR) at the FDA, said the surge in staff assigned to review EUA filings has worked to some benefit, claiming that the agency has rendered a decision in connection with 65 applications in the two weeks leading up to the Dec. 9 town hall.

Calling it a “a critical milestone in its fight against COVID-19,” Health Canada authorized the Pfizer Inc./Biontech SE COVID-19 vaccine for people age 16 or older.

The latest global regulatory news, changes and updates affecting medical devices and technologies, including: USPTO finalizes SAS rule, U.S. senators press case for permanent telehealth, CMS no fan of national coverage policy for Allomap, TGA posts guidance for class I tests, Marburg MCMs protected under PREP.

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Biolab Sciences, Cognitivecare, Colospan, Day Zero Diagnostics, Edap Tms, Htg Molecular Diagnostics, Keraderm, Menicon, Moderna, Mojo Vision, O2 Industries, Patient Power, Remedy Health Media, Roche, Sebia, Sight Diagnostics, Skinopathy, Sorrento Therapeutics, Vitalhub.