Therapeutic Products Act 2023 — New Legislative Framework for Medical Devicesnew-zealand📋 regulatory changes
Medical Device Act (RA 9711) and CDRRHR — Philippine Regulatory Frameworkphilippines📋 regulatory changes
Chestny ZNAK: Mandatory Digital Marking and Track-and-Trace for Medical Devicesrussia📋 regulatory changes
ISO 13485 and MDSAP Certificates Now Accepted for Dealer's Licence QMS Requirementssingapore📋 regulatory changes
UDI-K Compliance Deadlines by Device Grade — Unique Device Identification (Korea)south-korea📅 key dates
End of MedDO transitional provisions — CE-marked devices must be notified or registered in swissdamedswitzerland📅 key dates
Medical Device Act B.E. 2562 (2019) — Thailand's Modern Device Regulatory Frameworkthailand📋 regulatory changes
CE marking transitional arrangement ends — devices on Great Britain market must hold UKCA or approved body certificateunited-kingdom📅 key dates
QMSR — Quality Management System Regulation Transition from QSR (21 CFR Part 820)united-states📋 regulatory changes
UDI System — Unique Device Identification Requirements (21 CFR Parts 801 and 830)united-states📋 regulatory changes