Medical Device Global Market Access Podcast

Saudi Arabia SFDA Medical Device Advertising: New MDS-REQ 8 Requirements for Manufacturers	Medical Device Global Market Access	04:26
India's 2026 CDSCO Guidance on Medical Device Software (MDSW): Key Compliance Steps	Medical Device Global Market Access	05:08
FDA eMDR System Enhancements 2026: A Guide for Medical Device Manufacturers	Medical Device Global Market Access	05:39
China NMPA Draft GMP Inspection Guideline: Risk-Based Audits and Critical Check Items	Medical Device Global Market Access	05:12
ANVISA Medical Device Regulation 2026: Brazil and Chile's Technical Exchange and Its Impact	Medical Device Global Market Access	04:14
ANVISA Technovigilance Changes in Brazil: What to Expect After the Public Consultation	Medical Device Global Market Access	04:47
South Korea Medical Device Act 2026: MFDS QMS and Distribution Rule Changes	Medical Device Global Market Access	04:40
Saudi Arabia SFDA Risk Communication Guidance: What MDS-G-029 Means for Manufacturers	Medical Device Global Market Access	05:22
Health Canada Ministerial Reliance Order: Faster Market Access for Medical Devices	Medical Device Global Market Access	04:43
UK MHRA Draft Medical Device Regulations 2026: Key Changes and Timeline	Medical Device Global Market Access	05:10
EU REP Symbol Transition: Compliance Guide for Medical Device Labeling by 2031	Medical Device Global Market Access	05:05
Saudi Arabia SFDA Medical Device Bundling: Key Changes in Guidance MDS-G-028	Medical Device Global Market Access	05:19
Australia TGA UDI Requirements: High-Risk Device Compliance by July 1, 2026	Medical Device Global Market Access	04:55
EU MDR Well-Established Technologies (WET) Exemption: New Rules for Class III and IIb Devices	Medical Device Global Market Access	05:00
China NMPA BCI Classification Guidance: A New Framework for Neurotech Devices	Medical Device Global Market Access	05:39
FDA MDUFA VI Reauthorization: What to Expect for FY 2028-2032	Medical Device Global Market Access	05:37
Brazil's New e-Notivisa System: ANVISA's Overhaul of Medical Device Adverse Event Reporting	Medical Device Global Market Access	04:55
Brazil ANVISA Regulatory Reliance: IN 290/2024 Changes for Class III & IV Devices	Medical Device Global Market Access	04:53
EU MDCG 2026-4: SSCP Upload to EUDAMED for Class III & Implantable Devices	Medical Device Global Market Access	05:23
China NMPA Innovative Device Approvals Accelerate: Market Access in 2026	Medical Device Global Market Access	04:56
Australia's TGA UDI System: Preparing for the July 1, 2026 High-Risk Device Deadline	Medical Device Global Market Access	04:53
Japan PMDA SaMD Guidance 2026: AI/ML, Cybersecurity, and Classification Changes	Medical Device Global Market Access	05:23
India CDSCO Proposes Faster Medical Device License Timelines	Medical Device Global Market Access	05:17
South Korea Medical Device Act 2026: MFDS QMS and Distribution Changes	Medical Device Global Market Access	05:02
FDA AI Medical Device Draft Guidance 2026: Lifecycle Management and Submission Requirements	Medical Device Global Market Access	05:16
Health Canada MDEL Modernization Phase 2: 2026 Changes for Importers and Distributors	Medical Device Global Market Access	05:38
Australia TGA Classification Rule 5.5: Reclassification Changes for Medical Devices	Medical Device Global Market Access	05:20
Switzerland's Swissdamed: Mandatory Device and IVD Registration by July 2026	Medical Device Global Market Access	04:45
UK MHRA International Reliance: Navigating the Draft 2026 Medical Device Regulations	Medical Device Global Market Access	04:53
Brazil ANVISA Regulatory Reliance: June 2024 Update to IN 290/2024 Streamlines Class III/IV Device Review	Medical Device Global Market Access	04:58
China NMPA Post-Market Vigilance 2026: New Rules for Foreign Manufacturers	Medical Device Global Market Access	04:53
Saudi SFDA's 2026 AI Medical App Approval: A Global First for Vital Signs Monitoring	Medical Device Global Market Access	05:10
UK MHRA MDSAP Membership: Streamlining Audits for UK, US, Canada, and More	Medical Device Global Market Access	05:10
Singapore HSA COVID-19 IVD Reclassification: Class C Requirements from 2026	Medical Device Global Market Access	04:48
India CDSCO Proposes New Medical Device Import Rules for Hospitals (2026)	Medical Device Global Market Access	05:30
Health Canada's 2026 Hyperbaric Chamber Warning: Compliance for Unlicensed Devices	Medical Device Global Market Access	04:40
Health Canada MDEL Regulations 2026: What Importers and Foreign Manufacturers Need to Know	Medical Device Global Market Access	04:57
FDA AI Software Classification 2026: Class II and PCCP Rules for Imaging Devices	Medical Device Global Market Access	05:13
Brazil ANVISA SaMD Regulation Update: Preparing for Changes to RDC 657/2022	Medical Device Global Market Access	04:57
Singapore HSA's 2026 Medical Device Grouping Guidance: Key Changes in GN-12-1-R3	Medical Device Global Market Access	04:50

Saudi Arabia SFDA Medical Device Advertising: New MDS-REQ 8 Requirements for Manufacturers

Medical Device Global Market Access

04:26

India's 2026 CDSCO Guidance on Medical Device Software (MDSW): Key Compliance Steps

Medical Device Global Market Access

05:08

FDA eMDR System Enhancements 2026: A Guide for Medical Device Manufacturers

Medical Device Global Market Access

05:39

China NMPA Draft GMP Inspection Guideline: Risk-Based Audits and Critical Check Items

Medical Device Global Market Access

05:12