mpilo AI的动态

Enhancing mpilo AI to support diverse languages used within the healthcare system. Estonian ???? ? French ???? ? What language would you like mpilo AI to support? Tell us your choice in the comments! https://mpilo.ai

MEDICAL IP , a Korean AI-based digital twin solution provider, said it has entered a strategic partnership with HealthOnCloud, a local health startup, to expand its innovative lineup of AI-based medical solutions into the global market.

New MHRA guidance: Machine learning medical devices: transparency principles Guidelines for communicating clear and relevant information about machine learning-enabled medical devices.

?? Ensuring Compliance and Safety: Supporting AI-Enhanced Medical Devices Under the New AI Act ?? AI’s integration into healthcare is transforming the industry, but it comes with its own set of ethical and regulatory challenges. As the new AI Act rolls out across Europe, medical device manufacturers must meet strict new standards to ensure transparency, safety, and trust. In our latest blog post, we delve into: ?? The AI Act's goals and new requirements for AI-enhanced medical devices ?? How manufacturers can ensure compliance with IVDR and MDR regulations ?? The importance of data integrity, human oversight, and cybersecurity in medical AI systems Discover how SeproTec supports medical devices manufacturers with top-notch language and IP services, helping them navigate these regulatory landscapes and maintain quality standards. #AIACT #AIcompliance #MDR #IVDR #compliance #ISO13485 #riskassessment #safety #eu #eumarket #medicaldevices #diagnosticdevice #seprotec #translation #t9n #localization #l10n #interpreting #Lsps #languageservices #languageserviceprovider #multilingualsolutions #languagesolutions #professionaltranslation #patenttranslation #technicaltranslation #lifesciencestraslation

Yes, under the new #EUAIact, the world’s first comprehensive AI law, AI systems are subject to specific requirements aimed at ensuring #safety, #reliability, #fundamentalrights protection, #transparency and #ethics, detailing different rules for different #risklevels. In summary, the EU AI Act introduces specific obligations and standards that medical device manufacturers incorporating #AItechnologies must adhere to. For instance: ensuring #transparency in #AI algorithms applied to #healthcare and #medicaldevices

The difference between a regular autocorrect and a medical dictionary? ?? Explore how the latter recognizes, corrects, and suggests medical terms. Read more: https://lnkd.in/d7SszHyc #MedicalDictionary #TechInsights

Today’s Vendor Spotlight is… Nym What Nym does (Elion’s take): - Nym is an AI medical coding product that deciphers clinical language in patient charts and assigns ICD-10 and CPT codes to them using advanced machine learning and semantic technologies.? - They offer services for outpatient coding for both professional and facility charges, as well as inpatient coding for professional charges.? - Nym’s semantic and contextual understanding allows them to handle a range of medical coding scenarios from ancillary procedures like radiology and pathology to more complex situations such as emergency care and ambulatory procedures with minimal human intervention. Founded: 2018 Total Funding: $47.5M Leadership: Or Peles Core Differentiators (according to Nym): - Nym’s engine is the leading multi-specialty autonomous coding solution. - Our engine’s configurability and audit trails set us apart from other vendors. Learn more about Nym at https://lnkd.in/emJNwsQh. (And if you’re a healthcare vendor and want to get featured, claim and update your Elion profile today.)

https://lnkd.in/gYwE_vRb For some of us that are watch addicts we are fascinated by the complexity of all things outside a watch, but mostly inside. As fascinated as we are, it pales in comparison to the machines that make the movement for the watches. A trip to Switzerland will expose you to some of the most sophisticated manufacturing equipment on earth. The quality control belongs to many of this equipment, less human manual intervention, more validation of the process. Yes here comes the software, how can you not expect it. Now back to timeless FDA. So FDA has had more then its share of hits regulating software stand alone or as a medical device. Clinical decision software is that sophisticated "manufacturing” equipment used in making that decision to accept or reject that data. You can see the attempt of the agency to not really want to engage, after the PTSD of dealing with other software. Sounds more like good old natural human reaction than AI, and we know AI will ultimately rule, because it’s made from all those things human screwed up and a few that were successful.

Stay up-to-date with the ever-evolving medical device regulatory industry. Learn about these recent news updates: ??FDA AI Program: AI/ML Medical Device Research ? FDA Announces eMDR System Updates For more information on these updates, click here:?https://bit.ly/3WJ6NlE #RegulatoryNews #RegulatoryUpdates #MedicalDevice

Federation of State Medical Boards weighs in on <b>ethical</b> use of <b>AI</b> in clinical practice https://lnkd.in/eFx4Epg5