Try our Chrome extension
Easily add the current web-page from your browser directly into your changedetection.io tool, more great features coming soon!Changedetection.io needs your support!
You can help us by supporting changedetection.io on these platforms;
- Rate us at AlternativeTo.net
- Star us on GitHub
- Follow us at Twitter/X
- G2 Software reviews
- Check us out on LinkedIn
- And tell your friends and colleagues :)
The more popular changedetection.io is, the more time we can dedicate to adding amazing features!
Many thanks :)
changedetection.io team
Not yet seconds ago
False
Not yet seconds ago
18 hours ago
| Skip to main content * Services + Market Access + Human Factors Research & Design + Privacy & Security Services * Software + RAMS® o Product Classification o Smart Builder o RAMS® e-Learning o Registration Tracker o Regulatory Watch o Regulatory Intelligence o Regulatory Reports o Affiliated Services + OPUS™ o Subscriptions o eLearning o Documents o Tools * News + Regulatory Updates + Insights + Press Releases + Newsletters o RADAR o TalkingPoints * Resources + Market Data + Process Charts + eLearning Courses + Guides + Videos + Case Studies + White Papers + On-Demand Webinars + MDR Resource Center + IVDR Resource Center + LATAM Resource Center + Asia Resource Center * Events + Upcoming Webinars + On-Demand Webinars + Tradeshows * About + Careers + Locations + Our Consultants + ISO certificate * Newsletter Sign-up Explore all of UL Solutions Search Menu Industry Focus The healthcare industry is changing and we have the breadth of expertise to help you evolve with it. Overview Next Previous Services Comprehensive service offerings at every point in the product life cycle. Overview * Market Access * Human Factors Research & Design * Privacy & Security Services RAMS® A platform of digital products to improve, simplify and automate RA/QA activities Learn more OPUS™ Emergo by UL's new human factors tool - provides training, tools, and resources. Learn more Software Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools. Overview * RAMS® + Product Classification + Smart Builder + RAMS® e-Learning + Registration Tracker + Regulatory Watch + Regulatory Intelligence + Regulatory Reports + Affiliated Services * OPUS™ + Subscriptions + eLearning + Documents + Tools News The latest industry news and insights from our global team. View all * Regulatory Updates * Insights * Press Releases * Newsletters RADAR : Market Access Newsletter Stay informed with the most read RA/QA medical device newsletter. Sign up TalkingPoints : Human Factors Newsletter TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more. Sign up Resources Information and tools to advance your business. View all * Market Data * Process Charts * eLearning Courses * Guides * Videos * Case Studies * White Papers * On-Demand Webinars * MDR Resource Center * IVDR Resource Center * LATAM Resource Center * Asia Resource Center Events Learn from our experts through live events. View all * Upcoming Webinars * On-Demand Webinars * Tradeshows Next Previous About Our global consulting team works from 20+ offices on six continents. Overview * Careers * Locations * Our Consultants * ISO certificate Next Previous Switch Language * English * 한국어 * 日本語 * Deutsch * 繁體中文 News * Regulatory Updates * Insights * Press Releases * Newsletters Regulatory Updates Stay current with the most recent regulatory updates. Contact us * Home * News * Regulatory Updates Filter by Loading... Filter Search Submit Clear all X Filter by Service (0) Open * Human Factors Research & Design * Market Access Market (0) Open * Albania * Argentina * Australia * Bangladesh * Brazil * Canada * Colombia * Costa Rica * Egypt * Europe * France * Germany * Greater China * India * Indonesia * Israel * Japan * Kazakhstan * Malaysia * Mexico * Myanmar * New Zealand * Pakistan * Peru * Philippines * Saudi Arabia * Serbia * Singapore * South Africa * South Korea * Switzerland * The Netherlands * Turkey * Ukraine * United Kingdom * United States * Vietnam Reset all Done Reset all Pagination Pagination Page-1 Page 1 of 36 * Page-2 Page 2 * Page-3 Page 3 * Page-4 Page 4 * Page-5 Page 5 * Page-6 Page 6 * Page-7 Page 7 * Page-8 Page 8 * Page-9 Page 9 * Page-10 Page 10 * Page-11 Page 11 * Page-12 Page 12 * Page-13 Page 13 * Page-14 Page 14 * Page-15 Page 15 * Page-16 Page 16 * Page-17 Page 17 * Page-18 Page 18 * Page-19 Page 19 * Page-20 Page 20 * Page-21 Page 21 * Page-22 Page 22 * Page-23 Page 23 * Page-24 Page 24 * Page-25 Page 25 * Page-26 Page 26 * Page-27 Page 27 * Page-28 Page 28 * Page-29 Page 29 * Page-30 Page 30 * Page-31 Page 31 * Page-32 Page 32 * Page-33 Page 33 * Page-34 Page 34 * Page-35 Page 35 * Page-36 Page 36 * * Next page 431 results * new * Regulatory Update Dec 31, 2025 EU MDCG Issues Guidance on Post-Market Surveillance Under MDR, IVDR This month, the European Union Medical Device Coordination Group issued guidance on post-market surveillance under the... * new * Regulatory Update Dec 30, 2025 Updated European Manufacturer Incident Report Version 7.3.1 An updated Manufacturer Incident Report (MIR) version 7.3.1 form (SB-10781) was published on the European Commission... * Regulatory Update Dec 5, 2025 Malaysia MDA and Thai FDA Announce Pilot Regulatory Reliance Program The medical device regulators in Malaysia and Thailand have announced a pilot regulatory reliance program. * Regulatory Update Dec 3, 2025 The EU Commission Publishes Second Survey Results on Medical Device Availability Medical device availability is the subject of the newly released Second Survey report. * Regulatory Update Dec 2, 2025 European Legislation Published for First Four Modules of EUDAMED The European Commission published Decision 2025/2371, announcing the functionality of four EUDAMED modules. * Regulatory Update Dec 1, 2025 RAPS Regulatory Convergence 2025: Recommendations for Global Changes and Change Management The second in our series of RAPS 2025 coverage features global changes and change management. * Regulatory Update Nov 26, 2025 Japan Cabinet Order No. 362 Designates the US as Equivalent Regulatory Authority Japan's MHLW published Cabinet Order No. 362 of 2025, which revises the Order for Enforcement of the Pharmaceuticals and... * Regulatory Update Nov 14, 2025 Health Canada Expands Public Access to Clinical Data for Medical Devices New initiative gives stakeholders access to the clinical data behind regulatory decisions for Class III and IV medical... * Regulatory Update Nov 3, 2025 FDA CDRH Announces Priorities for Fiscal Year 2026 The U.S. government’s 2026 fiscal year (FY) commenced on Oct. 1. To start things off, the Food and Drug... * Regulatory Update Nov 3, 2025 The Medical Device Authority in Malaysia Releases Second Revised Guidance on Expanded Recognition Framework The Health Sciences Authority (HSA) of Singapore and the Thailand Food and Drug Administration (FDA) have now been added... * Regulatory Update Oct 28, 2025 Implementation of the European MIR Version 7.3.1 Form Appears to be Delayed until 2026 The European Commission has updated its website to signal a new revision of the Manufacturer Incident Report form, with... * Regulatory Update Oct 21, 2025 Malaysia MDA Announces Second Update to Policy on Recognition MDA reissues circular letter related to recognition implementation and enforcement policy. Pagination Page-1 Page 1 of 36 * Page-2 Page 2 * Page-3 Page 3 * Page-4 Page 4 * Page-5 Page 5 * Page-6 Page 6 * Page-7 Page 7 * Page-8 Page 8 * Page-9 Page 9 * Page-10 Page 10 * Page-11 Page 11 * Page-12 Page 12 * Page-13 Page 13 * Page-14 Page 14 * Page-15 Page 15 * Page-16 Page 16 * Page-17 Page 17 * Page-18 Page 18 * Page-19 Page 19 * Page-20 Page 20 * Page-21 Page 21 * Page-22 Page 22 * Page-23 Page 23 * Page-24 Page 24 * Page-25 Page 25 * Page-26 Page 26 * Page-27 Page 27 * Page-28 Page 28 * Page-29 Page 29 * Page-30 Page 30 * Page-31 Page 31 * Page-32 Page 32 * Page-33 Page 33 * Page-34 Page 34 * Page-35 Page 35 * Page-36 Page 36 * * Next page X Request information from our specialist Thanks for your interest in our products and services. Let's collect some information so we can connect you with the right person. Please wait… Characters remaining Thank you! We've received your request. We'll review your message carefully and get back to you as quickly as possible. To help ensure that you receive our reply, please add our domain @emergo.ul.com to your list of approved contacts. Ok * Services / Software + Market Access + Human Factors Research & Design + Privacy & Security Services + Software: RAMS® + Software: OPUS™ * Let's Connect + About + Contact Us + Office Locations + Newsletter Sign-up RAMS® A platform of digital products to improve, simplify and automate RA/QA activities. OPUSTM Emergo by UL's new human factors tool - provides training, tools, and resources. Choose a region Choose a region Select a regional website China (简体中文) © 2026 EMERGO by UL. All rights reserved. Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers. Impressum Online Policies About Cookies Data Subject Access Request Portal * Youtube * LinkedIn You are leaving the Emergo by UL website for an external site. Emergo by UL structures this activity to be distinct and separate from its conformity assessment bodies. | Skip to main content * Services + Market Access + Human Factors Research & Design + Privacy & Security Services * Software + RAMS® o Product Classification o Smart Builder o RAMS® e-Learning o Registration Tracker o Regulatory Watch o Regulatory Intelligence o Regulatory Reports o Affiliated Services + OPUS™ o Subscriptions o eLearning o Documents o Tools * News + Regulatory Updates + Insights + Press Releases + Newsletters o RADAR o TalkingPoints * Resources + Market Data + Process Charts + eLearning Courses + Guides + Videos + Case Studies + White Papers + On-Demand Webinars + MDR Resource Center + IVDR Resource Center + LATAM Resource Center + Asia Resource Center * Events + Upcoming Webinars + On-Demand Webinars + Tradeshows * About + Careers + Locations + Our Consultants + ISO certificate * Newsletter Sign-up Explore all of UL Solutions Search Menu Industry Focus The healthcare industry is changing and we have the breadth of expertise to help you evolve with it. Overview Next Previous Services Comprehensive service offerings at every point in the product life cycle. Overview * Market Access * Human Factors Research & Design * Privacy & Security Services RAMS® A platform of digital products to improve, simplify and automate RA/QA activities Learn more OPUS™ Emergo by UL's new human factors tool - provides training, tools, and resources. Learn more Software Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools. Overview * RAMS® + Product Classification + Smart Builder + RAMS® e-Learning + Registration Tracker + Regulatory Watch + Regulatory Intelligence + Regulatory Reports + Affiliated Services * OPUS™ + Subscriptions + eLearning + Documents + Tools News The latest industry news and insights from our global team. View all * Regulatory Updates * Insights * Press Releases * Newsletters RADAR : Market Access Newsletter Stay informed with the most read RA/QA medical device newsletter. Sign up TalkingPoints : Human Factors Newsletter TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more. Sign up Resources Information and tools to advance your business. View all * Market Data * Process Charts * eLearning Courses * Guides * Videos * Case Studies * White Papers * On-Demand Webinars * MDR Resource Center * IVDR Resource Center * LATAM Resource Center * Asia Resource Center Events Learn from our experts through live events. View all * Upcoming Webinars * On-Demand Webinars * Tradeshows Next Previous About Our global consulting team works from 20+ offices on six continents. Overview * Careers * Locations * Our Consultants * ISO certificate Next Previous Switch Language * English * 한국어 * 日本語 * Deutsch * 繁體中文 News * Regulatory Updates * Insights * Press Releases * Newsletters Regulatory Updates Stay current with the most recent regulatory updates. Contact us * Home * News * Regulatory Updates Filter by Loading... Filter Search Submit Clear all X Filter by Service (0) Open * Human Factors Research & Design * Market Access Market (0) Open * Albania * Argentina * Australia * Bangladesh * Brazil * Canada * Colombia * Costa Rica * Egypt * Europe * France * Germany * Greater China * India * Indonesia * Israel * Japan * Kazakhstan * Malaysia * Mexico * Myanmar * New Zealand * Pakistan * Peru * Philippines * Saudi Arabia * Serbia * Singapore * South Africa * South Korea * Switzerland * The Netherlands * Turkey * Ukraine * United Kingdom * United States * Vietnam Reset all Done Reset all Pagination Pagination Page-1 Page 1 of 36 * Page-2 Page 2 * Page-3 Page 3 * Page-4 Page 4 * Page-5 Page 5 * Page-6 Page 6 * Page-7 Page 7 * Page-8 Page 8 * Page-9 Page 9 * Page-10 Page 10 * Page-11 Page 11 * Page-12 Page 12 * Page-13 Page 13 * Page-14 Page 14 * Page-15 Page 15 * Page-16 Page 16 * Page-17 Page 17 * Page-18 Page 18 * Page-19 Page 19 * Page-20 Page 20 * Page-21 Page 21 * Page-22 Page 22 * Page-23 Page 23 * Page-24 Page 24 * Page-25 Page 25 * Page-26 Page 26 * Page-27 Page 27 * Page-28 Page 28 * Page-29 Page 29 * Page-30 Page 30 * Page-31 Page 31 * Page-32 Page 32 * Page-33 Page 33 * Page-34 Page 34 * Page-35 Page 35 * Page-36 Page 36 * * Next page 431 results * new * Regulatory Update Dec 31, 2025 EU MDCG Issues Guidance on Post-Market Surveillance Under MDR, IVDR This month, the European Union Medical Device Coordination Group issued guidance on post-market surveillance under the... * new * Regulatory Update Dec 30, 2025 Updated European Manufacturer Incident Report Version 7.3.1 An updated Manufacturer Incident Report (MIR) version 7.3.1 form (SB-10781) was published on the European Commission... * Regulatory Update Dec 5, 2025 Malaysia MDA and Thai FDA Announce Pilot Regulatory Reliance Program The medical device regulators in Malaysia and Thailand have announced a pilot regulatory reliance program. * Regulatory Update Dec 3, 2025 The EU Commission Publishes Second Survey Results on Medical Device Availability Medical device availability is the subject of the newly released Second Survey report. * Regulatory Update Dec 2, 2025 European Legislation Published for First Four Modules of EUDAMED The European Commission published Decision 2025/2371, announcing the functionality of four EUDAMED modules. * Regulatory Update Dec 1, 2025 RAPS Regulatory Convergence 2025: Recommendations for Global Changes and Change Management The second in our series of RAPS 2025 coverage features global changes and change management. * Regulatory Update Nov 26, 2025 Japan Cabinet Order No. 362 Designates the US as Equivalent Regulatory Authority Japan's MHLW published Cabinet Order No. 362 of 2025, which revises the Order for Enforcement of the Pharmaceuticals and... * Regulatory Update Nov 14, 2025 Health Canada Expands Public Access to Clinical Data for Medical Devices New initiative gives stakeholders access to the clinical data behind regulatory decisions for Class III and IV medical... * Regulatory Update Nov 3, 2025 FDA CDRH Announces Priorities for Fiscal Year 2026 The U.S. government’s 2026 fiscal year (FY) commenced on Oct. 1. To start things off, the Food and Drug... * Regulatory Update Nov 3, 2025 The Medical Device Authority in Malaysia Releases Second Revised Guidance on Expanded Recognition Framework The Health Sciences Authority (HSA) of Singapore and the Thailand Food and Drug Administration (FDA) have now been added... * Regulatory Update Oct 28, 2025 Implementation of the European MIR Version 7.3.1 Form Appears to be Delayed until 2026 The European Commission has updated its website to signal a new revision of the Manufacturer Incident Report form, with... * Regulatory Update Oct 21, 2025 Malaysia MDA Announces Second Update to Policy on Recognition MDA reissues circular letter related to recognition implementation and enforcement policy. Pagination Page-1 Page 1 of 36 * Page-2 Page 2 * Page-3 Page 3 * Page-4 Page 4 * Page-5 Page 5 * Page-6 Page 6 * Page-7 Page 7 * Page-8 Page 8 * Page-9 Page 9 * Page-10 Page 10 * Page-11 Page 11 * Page-12 Page 12 * Page-13 Page 13 * Page-14 Page 14 * Page-15 Page 15 * Page-16 Page 16 * Page-17 Page 17 * Page-18 Page 18 * Page-19 Page 19 * Page-20 Page 20 * Page-21 Page 21 * Page-22 Page 22 * Page-23 Page 23 * Page-24 Page 24 * Page-25 Page 25 * Page-26 Page 26 * Page-27 Page 27 * Page-28 Page 28 * Page-29 Page 29 * Page-30 Page 30 * Page-31 Page 31 * Page-32 Page 32 * Page-33 Page 33 * Page-34 Page 34 * Page-35 Page 35 * Page-36 Page 36 * * Next page X Request information from our specialist Thanks for your interest in our products and services. Let's collect some information so we can connect you with the right person. Please wait… Characters remaining Thank you! We've received your request. We'll review your message carefully and get back to you as quickly as possible. To help ensure that you receive our reply, please add our domain @emergo.ul.com to your list of approved contacts. Ok * Services / Software + Market Access + Human Factors Research & Design + Privacy & Security Services + Software: RAMS® + Software: OPUS™ * Let's Connect + About + Contact Us + Office Locations + Newsletter Sign-up RAMS® A platform of digital products to improve, simplify and automate RA/QA activities. OPUSTM Emergo by UL's new human factors tool - provides training, tools, and resources. Choose a region Choose a region Select a regional website China (简体中文) © 2026 EMERGO by UL. All rights reserved. Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers. Impressum Online Policies About Cookies Data Subject Access Request Portal * Youtube * LinkedIn You are leaving the Emergo by UL website for an external site. Emergo by UL structures this activity to be distinct and separate from its conformity assessment bodies. |
For now, Differences are performed on text, not graphically, only the latest screenshot is available.
Screenshot requires Playwright/WebDriver enabled