Medical Device Global Market Access
Today: #120 in Technology, India on our combined chart.
Chart positions today · United States
Not on the United States charts we track today.
Not on the United Kingdom charts we track today.
Not on the Canada charts we track today.
Not on the Australia charts we track today.
Not on the Germany charts we track today.
Not on the Brazil charts we track today.
Not on the Mexico charts we track today.
Not on the New Zealand charts we track today.
Not on the Ireland charts we track today.
Not on the Japan charts we track today.
Not on the Philippines charts we track today.
Not on the South Africa charts we track today.
If you like Medical Device Global Market Access, try…
Ranking history · United States
Latest episodes
-
Indonesia Halal Certification for Class A Medical Devices: The October 18, 2026 Deadline
October 25, 2026 · 5 minIndonesia is implementing mandatory Halal certification for Class A medical devices, with a critical deadline of October 18, 2026. This episode breaks down what the Halal Product Assurance Law means for manufacturers of low-risk devices…
-
Swissmedic swissdamed Importer Linking: April 1, 2027 Deadline for Medical Device Importers
October 24, 2026 · 4 minSwissmedic has activated the importer linking function in the swissdamed database as of October 1, 2026. This creates a new mandatory step for Swiss importers, who now have until April 1, 2027, to electronically link their actor…
-
EU Joint Clinical Assessment: First High-Risk Medical Devices Selected Under HTAR
October 23, 2026 · 5 minOn October 6, 2026, the European Commission selected the first group of high-risk medical devices to undergo a Joint Clinical Assessment (JCA) under the new EU Health Technology Assessment Regulation (HTAR). This episode explains what this…
-
Australia TGA Medical Device Fee Changes: What to Know for 2026 Audits
October 22, 2026 · 5 minAustralia's Therapeutic Goods Administration (TGA) has updated its guidance on fee reductions for medical device conformity and ARTG application audits. Effective October 1, 2026, these changes introduce a new fee model for design…
-
TGA AI Medical Scribe Regulation: When Clinical Software Becomes a Medical Device
October 21, 2026 · 5 minAustralia's Therapeutic Goods Administration (TGA) has clarified that many AI-powered digital scribes are considered medical devices, not simple administrative tools. Following a review published on October 16, 2023, the TGA found that 8…
Show 7 more episodesShow fewer episodes
-
Japan PMDA Generative AI Guidance: Key Review Points for Medical Device Manufacturers
October 20, 2026 · 5 minOn October 14, 2026, Japan's PMDA published its draft guidance, 'Review Points for Medical Devices Utilizing Generative AI.' This episode explores the key safety and performance evaluation criteria that manufacturers must understand to…
-
Health Canada Medical Device Shortage Guidance: Exceptional Importation and Sale Updates
October 19, 2026 · 5 minHealth Canada has released revised guidance on its framework for exceptional importation and sale of medical devices, effective October 16, 2026. This episode details the key clarifications for manufacturers facing potential device…
-
FDA Draft Guidance for Robotically Assisted Surgical Devices: Premarket Submission Insights
October 18, 2026 · 6 minOn October 9, 2026, the US FDA issued new draft guidance clarifying premarket submission requirements for robotically assisted surgical (RAS) devices. This episode breaks down the FDA's key recommendations for non-clinical testing…
-
FDA GenAI Medical Device Regulation: Key Considerations Before the October 19, 2026 Comment Deadline
October 17, 2026 · 5 minThe US FDA is considering a new 'total product lifecycle' approach for regulating medical devices that use Generative AI (GenAI). This episode breaks down the key elements of the FDA's discussion paper, including the unique risks the…
-
Singapore HSA-ACE Priority Track: Faster Market Access for Innovative Medical Devices
October 16, 2026 · 5 minSingapore's Health Sciences Authority (HSA) has announced a new priority pathway for innovative medical devices, launching in November 2026. The 'HSA-Agency for Care Effectiveness (ACE) Priority Track' enables simultaneous regulatory…
-
South Korea MFDS Proposes Faster Class II Medical Device Certification
October 15, 2026 · 5 minSouth Korea's Ministry of Food and Drug Safety (MFDS) has proposed a new one-stop certification and technical review process for Class II medical devices. This episode breaks down the amendment, announced on September 14, 2026, which aims…
-
Brazil ANVISA SaMD & AI Vigilance Rules: Mid-October 2026 Feedback Deadline
October 14, 2026 · 4 minBrazil's ANVISA has launched Public Call No. 4/2026 to revise its Tecnovigilância (post-market vigilance) framework, specifically seeking industry feedback on the challenges posed by Software as a Medical Device (SaMD) and AI. This episode…

Australia
Brazil
Canada
Germany
India
Ireland
Japan
Mexico
New Zealand
Philippines
South Africa
United Kingdom