ICYMI: EU medical providers have full access to COBRA-OS®. 🌍 With this groundbreaking aortic occlusion device being granted CE marking under the new EU Medical Device Regulations, COBRA-OS® has transformed how medical providers manage bleeding emergencies. Curious to learn more? Read the full article linked below. ✨ https://lnkd.in/ee6UQQHK #cobraos #medicalinnovation #cemarking #frontlinemedtech #patientcare #aorticocclusion #healthcarerevolution
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Stay compliant and stress-free in 2024 by understanding the latest medical device regulations. https://wix.to/vNJaIMy #RegulatoryUpdates #MedicalIndustry #MedicalDeviceRegulatory #MedicalDevice #MedicalDeviceManufacturing
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Timely Reporting of Medical Device Adverse Events Crucial #Classofmedicaldevice #MateriovigilanceProgrammeofIndia #MateriovigilanceProgrammeofIndia(MvPI) #MDR2017 #Medicaldeviceadverseevents #medicaldevicelicensing #medicaldeviceriskmanagement #MedicalDevices #MvPI #postmarketsurveillance(PMS)
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📢 Navigating the complexities of the European Union Medical Device Regulation (EUMDR) is crucial for ensuring compliance and market access. 🌐 Check out our comprehensive FAQs on the classification of medical devices under EUMDR to stay informed and compliant. From understanding risk levels to ensuring proper documentation, we've got you covered! 💼🔍 #EUMDR #MedicalDevices #HealthcareCompliance #RegulatoryAffairs #MedicalDeviceRegulation #DeviceClassification #HealthcareIndustry #MedicalDeviceManufacturing #EURegulations #PatientSafety
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Timely Reporting of Medical Device Adverse Events Crucial #Classofmedicaldevice #MateriovigilanceProgrammeofIndia #MateriovigilanceProgrammeofIndia(MvPI) #MDR2017 #Medicaldeviceadverseevents #medicaldevicelicensing #medicaldeviceriskmanagement #MedicalDevices #MvPI #postmarketsurveillance(PMS)
https://thehealthmaster.com/2024/05/17/timely-reporting-of-medical-device-adverse-events-crucial/?no_cache=1716219126
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❗ Important News for Medical Device Registration ❗ TFDA has implemented the new announcement on simplifying medical device registration. This includes exemptions for certain document submissions through either Full Pathway and Abridged Pathway. This change is designed to expedite business workflow and minimize paperwork. Stay updated with ATTOPOLIS for the latest global news! https://lnkd.in/dE7-aDZU #RegulatoryUpdate #AttopolisB2B #ArqonGroup #ComplianceUpdate #HealthcareInnovation #Thailand #MedicalDevices #HealthcareCompliance #BusinessGrowth #StreamlinedProcess #TFDA
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Dy. Director - Business Marketing @ ARQon | SG LOC | Marketing Strategy, Digital Marketing, Creative Communication | I help companies reduce marketing costs by 40%
𝐁𝐫𝐞𝐚𝐤𝐢𝐧𝐠 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐍𝐞𝐰𝐬 𝐟𝐫𝐨𝐦 𝐓𝐡𝐚𝐢𝐥𝐚𝐧𝐝❗ TFDA's new announcement simplifies medical device registration, reducing paperwork and speeding up workflows for both Full and Abridged Pathways. Stay ahead with these streamlined processes! #RegulatoryUpdate #AttopolisB2B #ArqonGroup #ComplianceUpdate #HealthcareInnovation #Thailand #MedicalDevices #HealthcareCompliance #BusinessGrowth #StreamlinedProcess #TFDA
❗ Important News for Medical Device Registration ❗ TFDA has implemented the new announcement on simplifying medical device registration. This includes exemptions for certain document submissions through either Full Pathway and Abridged Pathway. This change is designed to expedite business workflow and minimize paperwork. Stay updated with ATTOPOLIS for the latest global news! https://lnkd.in/dE7-aDZU #RegulatoryUpdate #AttopolisB2B #ArqonGroup #ComplianceUpdate #HealthcareInnovation #Thailand #MedicalDevices #HealthcareCompliance #BusinessGrowth #StreamlinedProcess #TFDA
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We know how tough it can be to navigate the complex and ever-changing world of medical device regulations. At Synergy, we’re here to make the process easier and help you get your medical device to market safely and successfully. Our tailored strategies are designed to minimize your company's risks, streamline compliance, and get your device into the hands of patients who need it. With our help, you can confidently bring your devices to market. Let’s connect today on a market access strategy for your next medical device. #MedicalDevices #RegulatoryCompliance #QualityAssurance
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US & Global Regulatory Affairs, Clinical Research & Quality Assurance Executive Leader (Life Sciences, Pharma/Biotech, cGMP, Medical Devices, IVDs), Board Member, Thought Leader, SME, Author & Educator.
We know how tough it can be to navigate the complex and ever-changing world of medical device regulations. At Synergy, we’re here to make the process easier and help you get your medical device to market safely and successfully. Our tailored strategies are designed to minimize your company's risks, streamline compliance, and get your device into the hands of patients who need it. With our help, you can confidently bring your devices to market. Let’s connect today on a market access strategy for your next medical device. #MedicalDevices #RegulatoryCompliance #QualityAssurance
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Changes to timelines in EU regulations will give #medicaldevice manufacturers some much-needed breathing room, but they can’t take their foot off the gas. With all the changes in the Medical Device Regulation, manufacturers need to make sure they’re on top of their submissions. Read more: https://hubs.ly/Q02s_wKm0. #MDR #medicaldevices #regulatorychanges #notifiedbodies #stateoftheart
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A key insight from our recent LinkedIn Live on the MDR/IVDR... Dr. Bassil Akra offers an expert comparison of the differences between the European and American approaches to medical device regulation. The full conversation with Dr. Akra is available on YouTube: https://lnkd.in/e--XcGzn Stay tuned for expert perspectives presented by #CommuniD – we’re committed to keeping you informed! #MedicalDeviceRegulation #IVDR #MDR
