D.med Software specializes in custom healthcare software development services and cybersecurity solutions. The company provides tailored medical software to meet specific requirements for medical devices.

D.med Software

D.med Software | 2,210 followers on LinkedIn. Innovative software and cybersecurity solutions for the medical device industry. | D.med Software is a fast-growing company with a focus on cybersecurity for embedded software and cloud applications for the medical industry.

Our company has over a decade of team expertise providing complete and robust solutions from low-level firmware and embedded applications to connected mobile/desktop apps and Cloud. We aim to build long-term partnerships with our customers, helping them to advance their medical devices while meeting their requirements in compliance with regulations.

Digital Marketing Specialist 📊 | Ecommerce Management🛒 | SEO Content Writer English & Spanish

Verónica Flores Burgess

Senior Embedded software developer, Engineer, R&D.

Jose M Navarrete Vicente

Senior Software Engineer en D.Med Software

Javier Ortega Carmona

Senior Project Manager I Certified Scrum Master (PSM I - PSM II)

Nuria Cruzado

𝗔𝘀 𝗖𝗢𝗠𝗣𝗔𝗠𝗘𝗗 𝟮𝟬𝟮𝟰 𝘄𝗶𝗻𝗱𝘀 𝗱𝗼𝘄𝗻, we would like to thank everyone who has made this experience so special - 𝗼𝘂𝗿 𝗰𝗼𝗹𝗹𝗲𝗮𝗴𝘂𝗲𝘀, 𝗰𝗹𝗶𝗲𝗻𝘁𝘀 𝗮𝗻𝗱 𝗻𝗲𝘄 𝗳𝗿𝗶𝗲𝗻𝗱𝘀. 🙏 It has been an honour to connect with so many brilliant minds dedicated to shaping the future of medical technology. We are committed to ensuring patient safety and delivering innovative, safe solutions. 𝗧𝗵𝗶𝘀 𝗶𝘀 𝘄𝗵𝗮𝘁 𝗴𝘂𝗶𝗱𝗲𝘀 𝗮𝗻𝗱 𝘂𝗻𝗶𝘁𝗲𝘀 𝘂𝘀 𝗶𝗻 𝗲𝘃𝗲𝗿𝘆 𝗰𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗶𝗼𝗻 𝘄𝗲 𝗽𝘂𝗿𝘀𝘂𝗲. We're always ready to pick up the conversation we couldn't finish or the one we'd like to continue. And you can still find us at our stand today! 📅 𝟭𝟭-𝟭𝟰 𝗡𝗼𝘃𝗲𝗺𝗯𝗲𝗿 𝟮𝟬𝟮𝟰. 📍 𝗠𝗲𝘀𝘀𝗲 𝗗ü𝘀𝘀𝗲𝗹𝗱𝗼𝗿𝗳, 𝗚𝗲𝗿𝗺𝗮𝗻𝘆. 🔹𝗛𝗮𝗹𝗹 𝟴𝗮/ 𝗡𝟭𝟭 Come along, and let's continue to build on these meaningful connections. 𝗧𝗵𝗮𝗻𝗸 𝘆𝗼𝘂 𝗳𝗼𝗿 𝗷𝗼𝗶𝗻𝗶𝗻𝗴 𝘂𝘀 𝗼𝗻 𝘁𝗵𝗶𝘀 𝗷𝗼𝘂𝗿𝗻𝗲𝘆. Together, we are pushing the boundaries of patient safety and innovation! #COMPAMED2024 #PatientSafety #MedTechInnovation #DmedTechnologies #ThankYou

D.med Technologies

🌟 𝗗𝗮𝘆 𝟯 𝗮𝘁 𝗖𝗢𝗠𝗣𝗔𝗠𝗘𝗗 𝟮𝟬𝟮𝟰: 𝗧𝗵𝗲 𝗝𝗼𝘂𝗿𝗻𝗲𝘆 𝗖𝗼𝗻𝘁𝗶𝗻𝘂𝗲𝘀! 🌟 ✨ What an incredible experience it’s been so far! Interacting with colleagues in our area of expertise has been a true pleasure, exchanging insights that have enriched us all and sparked new ideas. We’ve also had the privilege of engaging with clients, supporting them through our comprehensive 𝗲𝗻𝗱-𝘁𝗼-𝗲𝗻𝗱 𝗮𝗽𝗽𝗿𝗼𝗮𝗰𝗵 and adding value to their journey. 🙌 🚶♂️ 𝗛𝗮𝘃𝗲𝗻’𝘁 𝗺𝗮𝗱𝗲 𝗶𝘁 𝘁𝗼 𝗛𝗮𝗹𝗹 𝟴𝗔/𝗡𝟭𝟭 𝘆𝗲𝘁? We’re eagerly waiting for you to dive into some discussions on: 🔹 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗔𝗳𝗳𝗮𝗶𝗿𝘀 & 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗠𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁 🔹 𝗖𝘆𝗯𝗲𝗿𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲 🔹 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗔𝗳𝗳𝗮𝗶𝗿𝘀 & 𝗥𝗲𝘀𝗲𝗮𝗿𝗰𝗵 🔹 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿𝗶𝗻𝗴 𝗖𝗼𝗺𝗽𝗹𝗲𝘅 𝗠𝗲𝗰𝗵𝗮𝗻𝗶𝗰𝗮𝗹 𝗦𝘆𝘀𝘁𝗲𝗺𝘀 💬 𝗪𝗲’𝗱 𝗹𝗼𝘃𝗲 𝘁𝗼 𝗱𝗶𝘀𝗰𝘂𝘀𝘀 𝗵𝗼𝘄 𝗼𝘂𝗿 𝘁𝗮𝗶𝗹𝗼𝗿𝗲𝗱 𝘀𝗼𝗹𝘂𝘁𝗶𝗼𝗻𝘀 𝗰𝗮𝗻 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 𝘆𝗼𝘂𝗿 𝘃𝗶𝘀𝗶𝗼𝗻. 𝗦𝘁𝗼𝗽 𝗯𝘆 𝗮𝗻𝗱 𝗹𝗲𝘁’𝘀 𝗲𝘅𝗽𝗹𝗼𝗿𝗲 𝗼𝗽𝗽𝗼𝗿𝘁𝘂𝗻𝗶𝘁𝗶𝗲𝘀 𝘁𝗼𝗴𝗲𝘁𝗵𝗲𝗿! Two more days, and we’re just getting started. Don’t miss out—let’s connect and shape the future of Medtech together! #COMPAMED2024 #Innovation #RegulatoryAffairs #Cybersecurity #ClinicalResearch #MedicalTechnology #MEDICA #Medtech

🚀 𝗧𝗵𝗲 𝗗𝗮𝘆 𝗛𝗮𝘀 𝗖𝗼𝗺𝗲: 𝗪𝗲'𝗿𝗲 𝗮𝘁 𝗖𝗢𝗠𝗣𝗔𝗠𝗘𝗗 𝟮𝟬𝟮𝟰! 🚀 We’re excited to share that D.med Technologies has officially arrived at 𝗖𝗢𝗠𝗣𝗔𝗠𝗘𝗗 𝟮𝟬𝟮𝟰 in 𝗗𝘂𝘀𝘀𝗲𝗹𝗱𝗼𝗿𝗳, where 𝗶𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻 𝗶𝗻 𝗺𝗲𝗱𝗶𝗰𝗮𝗹 𝗱𝗲𝘃𝗶𝗰𝗲 𝗱𝗲𝘃𝗲𝗹𝗼𝗽𝗺𝗲𝗻𝘁 takes center stage. We are here to 𝗲𝗺𝗽𝗼𝘄𝗲𝗿 𝗺𝗲𝗱𝗶𝗰𝗮𝗹 𝗱𝗲𝘃𝗶𝗰𝗲 𝗺𝗮𝗻𝘂𝗳𝗮𝗰𝘁𝘂𝗿𝗲𝗿𝘀 with innovative solutions, strict regulatory compliance, and superior 𝗽𝗿𝗼𝗱𝘂𝗰𝘁 𝘀𝗮𝗳𝗲𝘁𝘆. With our comprehensive, 𝗲𝗻𝗱-𝘁𝗼-𝗲𝗻𝗱 𝗮𝗽𝗽𝗿𝗼𝗮𝗰𝗵, we ensure that your devices not only meet all 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗿𝗲𝗾𝘂𝗶𝗿𝗲𝗺𝗲𝗻𝘁𝘀 but also 𝗺𝗮𝘅𝗶𝗺𝗶𝘀𝗲 𝗽𝗿𝗼𝗳𝗶𝘁𝗮𝗯𝗶𝗹𝗶𝘁𝘆. 💡 𝗛𝗼𝘄 𝗪𝗲 𝗖𝗮𝗻 𝗚𝘂𝗶𝗱𝗲 𝗬𝗼𝘂: 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗔𝗳𝗳𝗮𝗶𝗿𝘀 & 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗠𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁: With our expert guidance, navigate the complexities of MDR (EU) and FDA (US) regulations. From a seamless MDD-to-MDR transition to proactive post-market surveillance, we have you cover every step. 𝗖𝘆𝗯𝗲𝗿𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲: In an era where patient safety is critical, we integrate robust cybersecurity measures throughout your product's lifecycle—from initial design to post-market—to protect data and ensure device security. 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗔𝗳𝗳𝗮𝗶𝗿𝘀 & 𝗥𝗲𝘀𝗲𝗮𝗿𝗰𝗵: Our tailored regulatory support streamlines every phase of the clinical trial process. With high-quality lab services and efficient, end-to-end clinical expertise, we help accelerate your product’s path to approval. 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿𝗶𝗻𝗴 𝗖𝗼𝗺𝗽𝗹𝗲𝘅 𝗠𝗲𝗰𝗵𝗮𝗻𝗶𝗰𝗮𝗹 𝗦𝘆𝘀𝘁𝗲𝗺𝘀: We specialise in precision-driven development, customised testing frameworks, and advanced prototyping. Our solutions enhance device robustness, reliability, and efficiency, giving you a competitive edge. At D.med Technologies, we support your vision with holistic solutions, unparalleled expertise, and a genuine commitment to collaboration. 🔗𝗟𝗲𝘁’𝘀 𝗦𝗵𝗮𝗽𝗲 𝘁𝗵𝗲 𝗙𝘂𝘁𝘂𝗿𝗲 𝗧𝗼𝗴𝗲𝘁𝗵𝗲𝗿! Join us in 𝗛𝗮𝗹𝗹 𝟴𝗔 / 𝗕𝗼𝗼𝘁𝗵 𝗡𝟭𝟭 and discover how we can transform your challenges into opportunities. Your success is our mission! #COMPAMED #MedTech #MedicalDevices #HealthcareInnovation #LifeSciences #MedTechSolutions #RegulatoryCompliance #MDR #FDA #Cybersecurity #ClinicalResearch #Engineering #MedicalTechnology #Innovation #Dusseldorf #FutureOfHealthcare #MedicalDeviceDevelopment #DigitalHealth #HealthTech

🔐 #Cybersecurity 𝐞𝐱𝐩𝐞𝐫𝐭𝐬 𝐚𝐫𝐞 𝐧𝐨𝐭 𝐣𝐮𝐬𝐭 𝐭𝐢𝐜𝐤𝐢𝐧𝐠 𝐛𝐨𝐱𝐞𝐬 𝐟𝐨𝐫 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞… 🥷They are 𝐜𝐫𝐞𝐚𝐭𝐢𝐧𝐠 𝐚 𝐬𝐞𝐜𝐮𝐫𝐞, 𝐫𝐞𝐥𝐢𝐚𝐛𝐥𝐞, 𝐚𝐧𝐝 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐭 𝐟𝐨𝐮𝐧𝐝𝐚𝐭𝐢𝐨𝐧 for your #medical_device_software that withstands 𝐭𝐨𝐝𝐚𝐲’𝐬 𝐭𝐡𝐫𝐞𝐚𝐭𝐬 𝐚𝐧𝐝 𝐭𝐨𝐦𝐨𝐫𝐫𝐨𝐰’𝐬 𝐜𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬. 𝐇𝐞𝐫𝐞’𝐬 𝐰𝐡𝐞𝐫𝐞 #IEC 𝟖𝟏𝟎𝟎𝟏-𝟓-𝟏 𝐬𝐭𝐞𝐩𝐬 𝐢𝐧 👇 🛡️ 𝐇𝐨𝐰 𝐝𝐨 𝐰𝐞 𝐞𝐧𝐬𝐮𝐫𝐞 𝐞𝐧𝐝-𝐭𝐨-𝐞𝐧𝐝 𝐬𝐞𝐜𝐮𝐫𝐢𝐭𝐲 𝐭𝐡𝐫𝐨𝐮𝐠𝐡𝐨𝐮𝐭 𝐭𝐡𝐞 𝐬𝐨𝐟𝐭𝐰𝐚𝐫𝐞 𝐥𝐢𝐟𝐞𝐜𝐲𝐜𝐥𝐞? 𝐈𝐄𝐂 𝟖𝟏𝟎𝟎𝟏-𝟓-𝟏 𝐩𝐫𝐨𝐯𝐢𝐝𝐞𝐬 𝐚 𝐬𝐭𝐫𝐮𝐜𝐭𝐮𝐫𝐞𝐝 𝐟𝐫𝐚𝐦𝐞𝐰𝐨𝐫𝐤 that prescribes defined processes, activities and tasks throughout the 𝐬𝐨𝐟𝐭𝐰𝐚𝐫𝐞 𝐥𝐢𝐟𝐞𝐜𝐲𝐜𝐥𝐞 to increase its security, from initial concept to retirement. This ensures that robust risk management is built into every phase of development, 𝐦𝐢𝐭𝐢𝐠𝐚𝐭𝐢𝐧𝐠 𝐬𝐞𝐜𝐮𝐫𝐢𝐭𝐲 𝐫𝐢𝐬𝐤𝐬 𝐚𝐧𝐝 𝐯𝐮𝐥𝐧𝐞𝐫𝐚𝐛𝐢𝐥𝐢𝐭𝐢𝐞𝐬 𝐛𝐞𝐟𝐨𝐫𝐞 𝐭𝐡𝐞𝐲 𝐛𝐞𝐜𝐨𝐦𝐞 #security_threats . 🕵️♂️ 𝐇𝐨𝐰 𝐝𝐨 𝐰𝐞 𝐦𝐚𝐢𝐧𝐭𝐚𝐢𝐧 𝐭𝐡𝐞 𝐬𝐞𝐜𝐮𝐫𝐢𝐭𝐲 𝐨𝐟 𝐭𝐡𝐞 𝐬𝐨𝐟𝐭𝐰𝐚𝐫𝐞 𝐚𝐟𝐭𝐞𝐫 𝐝𝐞𝐩𝐥𝐨𝐲𝐦𝐞𝐧𝐭?? The standard requires a comprehensive 𝐩𝐨𝐬𝐭-𝐦𝐚𝐫𝐤𝐞𝐭 𝐦𝐚𝐢𝐧𝐭𝐞𝐧𝐚𝐧𝐜𝐞 𝐩𝐥𝐚𝐧. Launching a secure product is not enough; continuous monitoring, updating, and risk assessment are essential to maintaining software integrity against evolving cybersecurity threats. 𝐈𝐄𝐂 𝟖𝟏𝟎𝟎𝟏-𝟓-𝟏 𝐨𝐮𝐭𝐥𝐢𝐧𝐞𝐬 𝐭𝐡𝐞 𝐩𝐫𝐨𝐜𝐞𝐬𝐬𝐞𝐬 𝐧𝐞𝐞𝐝𝐞𝐝 𝐭𝐨 𝐞𝐧𝐬𝐮𝐫𝐞 𝐜𝐨𝐧𝐭𝐢𝐧𝐮𝐨𝐮𝐬 𝐦𝐨𝐧𝐢𝐭𝐨𝐫𝐢𝐧𝐠 𝐨𝐟 𝐭𝐡𝐞 𝐩𝐫𝐨𝐝𝐮𝐜𝐭'𝐬 𝐬𝐞𝐜𝐮𝐫𝐢𝐭𝐲 𝐚𝐧𝐝 𝐭𝐡𝐚𝐭 𝐮𝐩𝐝𝐚𝐭𝐞𝐬 𝐝𝐨𝐧'𝐭 𝐜𝐨𝐦𝐩𝐫𝐨𝐦𝐢𝐬𝐞 𝐬𝐞𝐜𝐮𝐫𝐢𝐭𝐲 𝐨𝐫 𝐩𝐞𝐫𝐟𝐨𝐫𝐦𝐚𝐧𝐜𝐞. 🧑💻𝐇𝐨𝐰 𝐜𝐚𝐧 𝐰𝐞 𝐦𝐞𝐞𝐭 𝐫𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐫𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬 𝐚𝐧𝐝 𝐞𝐧𝐬𝐮𝐫𝐞 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞 𝐰𝐡𝐢𝐥𝐞 𝐢𝐧𝐧𝐨𝐯𝐚𝐭𝐢𝐧𝐠? 𝐈𝐄𝐂 𝟖𝟏𝟎𝟎𝟏-𝟓-𝟏 𝐬𝐢𝐦𝐩𝐥𝐢𝐟𝐢𝐞𝐬 𝐫𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞 by harmonizing the development process, helping you to meet the expectations of bodies such as the FDA and MDR. By embedding cybersecurity and risk management into your workflow, you streamline the approval process and future-proof your software against increasingly stringent regulations. Let us show you 𝐭𝐡𝐞 𝐁𝐥𝐮𝐞𝐩𝐫𝐢𝐧𝐭 𝐟𝐨𝐫 𝐒𝐚𝐟𝐞 𝐚𝐧𝐝 𝐄𝐟𝐟𝐞𝐜𝐭𝐢𝐯𝐞 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐒𝐨𝐟𝐭𝐰𝐚𝐫𝐞 👉 dmed-software.com/contact #Cybersecurity #MedicalSoftware #DeviceSafety #RegulatoryCompliance #RiskManagement #SoftwareLifecycle #SSDLC #HealthTech #SoftwareDevelopment #DeviceSafety #DigitalHealth #IomT #DataSecurity #PatientSafety #MDR #FDACompliance #Cybersecurity

💡𝗨𝗻𝗹𝗼𝗰𝗸 𝗬𝗼𝘂𝗿 𝗣𝗼𝘁𝗲𝗻𝘁𝗶𝗮𝗹 – 𝗝𝗼𝗶𝗻 𝗢𝘂𝗿 𝗙𝗮𝘀𝘁-𝗚𝗿𝗼𝘄𝗶𝗻𝗴 𝗧𝗲𝗮𝗺! 📈 We are excited to announce that we continue to expand and are currently looking for talented and motivated professionals to fill the following roles: 🔹 𝗝𝘂𝗻𝗶𝗼𝗿 𝗠𝗮𝗿𝗸𝗲𝘁𝗶𝗻𝗴 𝗦𝗽𝗲𝗰𝗶𝗮𝗹𝗶𝘀𝘁 🔹 𝗘𝗹𝗲𝗰𝘁𝗿𝗼𝗻𝗶𝗰 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 If you're passionate about innovation, eager to grow, and ready to make an impact, we want to hear from you! At D.med Software we offer a dynamic work environment, opportunities for professional development, and a chance to work with a supportive and driven team. 👉𝗔𝗽𝗽𝗹𝘆 𝗻𝗼𝘄 𝗮𝗻𝗱 𝗷𝗼𝗶𝗻 𝗼𝘂𝗿 𝘁𝗵𝗿𝗶𝘃𝗶𝗻𝗴 𝘀𝘂𝗰𝗰𝗲𝘀𝘀! dmed-software.com/careers #Hiring #Marketing #Engineering #JoinOurTeam #CareerOpportunity #ElectronicEngineer

🔍𝐖𝐡𝐚𝐭 𝐢𝐬 #𝐈𝐨𝐌𝐓 ? The future of healthcare is connected! 🛜 Discover how the Internet of Medical Things (IoMT) is revolutionising patient care, bringing faster diagnosis, personalized treatment, and safer medical processes. At D.med Software , we share your mission to protect patients, secure the future of medical devices and ensure that our innovations keep healthcare safe and efficient. 👇 https://lnkd.in/e4sKXmma #IoMT #Cybersecurity #PatientSafety #HealthcareInnovation #DigitalTransformation #MedicalTechnology #DigitalHealth #MedicalDevices #HealthcareInnovation #CybersecurityForHealthcare #MedTech #RegulatoryAffairs #PremarketApproval #QMSCompliance #FDARegulations

🌟 𝐓𝐞𝐚𝐦 𝐁𝐮𝐢𝐥𝐝𝐢𝐧𝐠 𝐃𝐚𝐲 🌟 What an incredible experience at D.med Software during our recent team-building day! 🎉 Our wonderful colleague, Yangyang Li Li, took us on a fascinating 𝐜𝐮𝐥𝐭𝐮𝐫𝐚𝐥 𝐣𝐨𝐮𝐫𝐧𝐞𝐲 𝐭𝐡𝐫𝐨𝐮𝐠𝐡 𝐂𝐡𝐢𝐧𝐚. The day started with a delightful introduction to the world of Chinese teas, where we tasted and learned about different varieties 🍵. Then, we indulged in some traditional Chinese pastries 🥮, which were just as delicious as they were unique. The highlight of the day? Trying our hand at Chinese calligraphy! 🖌️ Each of us had the chance to write our names in Chinese, an extraordinary and creative moment. It was a beautiful day filled with learning, laughter, and 𝐭𝐞𝐚𝐦 𝐬𝐩𝐢𝐫𝐢𝐭! We're already looking forward to our next cultural adventure together. 🌍💼 #TeamBuilding #CulturalExperience #ChineseCulture #Teambonding #Diversity

🚨 𝗗.𝗺𝗲𝗱 𝗦𝗼𝗳𝘁𝘄𝗮𝗿𝗲 & 𝗗𝗘𝗞𝗥𝗔 𝗷𝗼𝗶𝗻 𝗳𝗼𝗿𝗰𝗲𝘀 𝘁𝗼 𝘀𝘁𝗿𝗲𝗻𝗴𝘁𝗵𝗲𝗻 𝗠𝗲𝗱𝗶𝗰𝗮𝗹 𝗖𝘆𝗯𝗲𝗿𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 🚨 D.med Software , 𝗮 𝘀𝗽𝗲𝗰𝗶𝗮𝗹𝗶𝘀𝘁 𝗶𝗻 𝗰𝘆𝗯𝗲𝗿𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝗳𝗼𝗿 𝗺𝗲𝗱𝗶𝗰𝗮𝗹 𝗱𝗲𝘃𝗶𝗰𝗲𝘀, has joined forces with DEKRA Digital & Product Solutions , 𝗮 𝗴𝗹𝗼𝗯𝗮𝗹 𝗹𝗲𝗮𝗱𝗲𝗿 𝗶𝗻 𝘁𝗲𝘀𝘁𝗶𝗻𝗴, 𝗶𝗻𝘀𝗽𝗲𝗰𝘁𝗶𝗼𝗻, 𝗮𝗻𝗱 𝗰𝗲𝗿𝘁𝗶𝗳𝗶𝗰𝗮𝘁𝗶𝗼𝗻, to tackle growing cyber threats in healthcare and beyond. This strategic #partnership will drive innovation in cybersecurity solutions, helping industries like automotive, industrial, and IoT stay ahead of evolving regulations. By leveraging their combined expertise, the partnership will focus on 𝗿𝗮𝗶𝘀𝗶𝗻𝗴 𝗮𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀, 𝗽𝗿𝗼𝗺𝗼𝘁𝗶𝗻𝗴 𝗰𝘆𝗯𝗲𝗿𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝘁𝗿𝗮𝗶𝗻𝗶𝗻𝗴, 𝗮𝗻𝗱 𝗰𝗼𝗻𝗱𝘂𝗰𝘁𝗶𝗻𝗴 𝗶𝗻𝗱𝗲𝗽𝗲𝗻𝗱𝗲𝗻𝘁 𝗮𝘀𝘀𝗲𝘀𝘀𝗺𝗲𝗻𝘁𝘀 𝘁𝗼 𝗲𝗻𝘀𝘂𝗿𝗲 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗰𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲. Together, DEKRA Digital & Product Solutions and D.med Software are committed to protecting critical infrastructure and safeguarding sensitive data. 🌐 𝗧𝗵𝗶𝘀 𝗰𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗶𝗼𝗻 𝗶𝘀 𝘀𝗲𝘁 𝘁𝗼 𝗿𝗲𝗱𝗲𝗳𝗶𝗻𝗲 𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝗶𝗻 𝗮 𝗱𝗶𝗴𝗶𝘁𝗮𝗹𝗹𝘆 𝗰𝗼𝗻𝗻𝗲𝗰𝘁𝗲𝗱 𝘄𝗼𝗿𝗹𝗱!💡🔒 https://lnkd.in/egCAqvGA #CyberSecurity #MedicalTechnology #IoT #Innovation

🔐 𝗖𝘂𝗿𝗶𝗼𝘂𝘀 𝗮𝗯𝗼𝘂𝘁 𝗵𝗼𝘄 𝗦𝗧𝗥𝗜𝗗𝗘 𝗰𝗮𝗻 𝗲𝗹𝗲𝘃𝗮𝘁𝗲 𝘁𝗵𝗲 𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝗼𝗳 𝘆𝗼𝘂𝗿 𝗺𝗲𝗱𝗶𝗰𝗮𝗹 𝗱𝗲𝘃𝗶𝗰𝗲𝘀? #Cybersecurity is a critical aspect of #medical_device safety in a world with evolving digital threats. STRIDE is the preferred approach for identifying threats in threat model diagrams. At D.med Software , we specialise in integrating advanced cybersecurity frameworks like STRIDE into the development process to secure your devices. Each data flow is examined for potential risks across six threat categories: 🎭 Spoofing 🔧 Tampering ❌ Repudiation 🕵️ Information disclosure (privacy breaches or data leaks) ⛔ Denial of service 👑 Elevation of privilege Then follow these steps to see how #STRIDE enhances the security of your device, going beyond traditional security measures to provide a comprehensive framework for identifying and addressing potential vulnerabilities: 𝗠𝗶𝘁𝗶𝗴𝗮𝘁𝗶𝗼𝗻 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀: Helps developers understand and plan for specific threats and tailor security measures accordingly. 𝗦𝗲𝗰𝘂𝗿𝗶𝘁𝘆 𝗗𝗲𝘀𝗶𝗴𝗻: Integrates security considerations into the design phase, building a robust defence from the ground up. 𝗖𝗼𝗻𝘁𝗶𝗻𝘂𝗼𝘂𝘀 𝗜𝗺𝗽𝗿𝗼𝘃𝗲𝗺𝗲𝗻𝘁: Facilitates ongoing assessment and improvement of security measures, to keep pace with evolving threats. Use this method to improve the cybersecurity of your devices and systems. Notified bodies and authorities will take note of how threat modelling is incorporated into your technical documentation. Partner with us to enhance the security of your device, streamline compliance, and build trust with regulators and customers alike. 𝗟𝗲𝘁'𝘀 𝘀𝗲𝗰𝘂𝗿𝗲 𝘆𝗼𝘂𝗿 𝗳𝘂𝘁𝘂𝗿𝗲 𝗶𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻𝘀 𝘁𝗼𝗴𝗲𝘁𝗵𝗲𝗿! 👉 https://lnkd.in/eAryHvPM #MedicalDevices #HealthTechSecurity #securitydesign #DigitalHealthSafety #threatmodelling

🌟 𝗪𝗵𝘆 𝗱𝗼𝗲𝘀 𝘁𝗵𝗲 𝗙𝗗𝗔 𝗰𝗮𝗿𝗲 𝗮𝗯𝗼𝘂𝘁 𝗵𝗼𝘄 𝘄𝗲 𝗯𝘂𝗶𝗹𝗱 𝗼𝘂𝗿 𝘀𝗼𝗳𝘁𝘄𝗮𝗿𝗲? 🌟 As industry professionals, we all understand that the development of medical device software carries immense responsibilities. But why does the FDA emphasize so much on how we build our software? Here’s why every stakeholder in the medical device sector should care: 𝗣𝗮𝘁𝗶𝗲𝗻𝘁 𝗦𝗮𝗳𝗲𝘁𝘆: Our top priority. Faulty software can lead to critical failures—misdiagnoses, incorrect dosing, or worse. Ensuring our software is built to the highest standards is not just regulatory, 𝗶𝘁'𝘀 𝗮 𝗺𝗼𝗿𝗮𝗹 𝗼𝗯𝗹𝗶𝗴𝗮𝘁𝗶𝗼𝗻. 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗮𝗻𝗱 𝗥𝗲𝗹𝗶𝗮𝗯𝗶𝗹𝗶𝘁𝘆: Robust software development practices mean devices work flawlessly, delivering consistent, reliable patient outcomes.𝗜𝘁'𝘀 𝗮𝗯𝗼𝘂𝘁 𝗯𝘂𝗶𝗹𝗱𝗶𝗻𝗴 𝘁𝗿𝘂𝘀𝘁 𝘄𝗶𝘁𝗵 𝗲𝘃𝗲𝗿𝘆 𝗱𝗲𝘃𝗶𝗰𝗲 𝘄𝗲 𝗿𝗲𝗹𝗲𝗮𝘀𝗲. 𝗖𝘆𝗯𝗲𝗿𝘀𝗲𝗰𝘂𝗿𝗶𝘁𝘆: In an era where device connectivity is the norm, safeguarding patient data and device functionality through stringent cybersecurity measures is crucial. 𝗔 𝗯𝗿𝗲𝗮𝗰𝗵 𝗶𝘀 𝗻𝗼𝘁 𝗷𝘂𝘀𝘁 𝗮 𝗹𝗼𝘀𝘀 𝗼𝗳 𝗱𝗮𝘁𝗮 𝗯𝘂𝘁 𝗮 𝗽𝗼𝘁𝗲𝗻𝘁𝗶𝗮𝗹 𝘁𝗵𝗿𝗲𝗮𝘁 𝘁𝗼 𝗹𝗶𝗳𝗲. 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲: Staying aligned with FDA guidelines and the IEC 62304 standard, isn’t just about avoiding penalties—it’s about proving 𝗼𝘂𝗿 𝗰𝗼𝗺𝗺𝗶𝘁𝗺𝗲𝗻𝘁 𝘁𝗼 𝗴𝗹𝗼𝗯𝗮𝗹 𝘀𝗮𝗳𝗲𝘁𝘆 𝗮𝗻𝗱 𝗾𝘂𝗮𝗹𝗶𝘁𝘆 𝘀𝘁𝗮𝗻𝗱𝗮𝗿𝗱𝘀. 𝗜𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻 𝘄𝗶𝘁𝗵 𝗜𝗻𝘁𝗲𝗴𝗿𝗶𝘁𝘆: As technology evolves, so should our approaches to integrating and safeguarding new tech. Adhering to FDA standards helps ensure that innovations enhance, not compromise, patient safety. Every step in our 𝘀𝗼𝗳𝘁𝘄𝗮𝗿𝗲 𝗱𝗲𝘃𝗲𝗹𝗼𝗽𝗺𝗲𝗻𝘁 𝗹𝗶𝗳𝗲𝗰𝘆𝗰𝗹𝗲 𝗺𝗮𝘁𝘁𝗲𝗿𝘀—𝗳𝗿𝗼𝗺 𝗱𝗲𝘀𝗶𝗴𝗻 𝘁𝗼 𝗱𝗲𝗽𝗹𝗼𝘆𝗺𝗲𝗻𝘁. Let’s continue to lead with safety, innovate with purpose, and build with integrity. Because at the end of the day, 𝗼𝘂𝗿 𝘄𝗼𝗿𝗸 𝗵𝗮𝘀 𝘁𝗵𝗲 𝘂𝗻𝗶𝗾𝘂𝗲 𝗽𝗼𝘄𝗲𝗿 𝘁𝗼 𝘀𝗮𝘃𝗲 𝗹𝗶𝘃𝗲𝘀.❤️ At D.med Software , we specialise in developing FDA-compliant medical device software that embodies these principles to ensure patient safety, cybersecurity, and innovation integrity. 𝗙𝗿𝗼𝗺 𝗰𝗼𝗻𝗰𝗲𝗽𝘁 𝘁𝗼 𝗱𝗲𝗽𝗹𝗼𝘆𝗺𝗲𝗻𝘁. 𝗗𝗶𝘀𝗰𝗼𝘃𝗲𝗿 𝗵𝗼𝘄 𝘄𝗲 𝗰𝗮𝗻 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 𝘆𝗼𝘂𝗿 𝗻𝗲𝘅𝘁 𝗽𝗿𝗼𝗷𝗲𝗰𝘁 👉 https://lnkd.in/eXu3YtZP #MedicalDevices #HealthTech #FDACompliance #Cybersecurity #PatientSafety #SoftwareDevelopmen t #Innovation #MedicalDeviceSafety

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