Our team of automation engineers can help you take your production line to the next level with our custom automation builds. We can create production lines from the ground up, with complete or partial automation, but also demonstrate our adaptability by integrating automation into your existing production lines. Our automation experts tailor each step of the automation process to your specific product and production needs. Reach out to us today and learn more at: https://lnkd.in/enAdqatu. We are a leading vertically integrated medical device contract manufacturer with an agile and scalable global footprint that includes Costa Rica, the Dominican Republic, and Ireland.
Biomerics’ Post
More Relevant Posts
-
Read how one our Rockwell Automation Gold OEM Partners delivered an innovative solution to a Life Sciences Medical Device Company in what had been a long standing manual process. This solution helped define a new “art of the possible” for a customer application that had not changed in many years. It all starts with asking the right expert the question, “what more can I achieve?” #RockwellAutomation, #DigitalTransformation, #Invio https://lnkd.in/gWihVAMu
To view or add a comment, sign in
-
Maintaining product quality and reliability is essential in manufacturing medical devices. An especially important topic is verification and validation (V&V)—the pivotal processes in the development and manufacturing of medical electrodes. It ensures: 📌 product performance 📌 regulatory compliance 📌 risk mitigation 📌 customer satisfaction Read more information on the topic in Screentec Oy’s recent publication. 👇👇👇 https://lnkd.in/d78rXcF8 Laura Kallo Antti TauriainenMikko Paakkolanvaara Jani Sutinen Hamza KHALLOK
To view or add a comment, sign in
-
Don't miss Robotiq Automation Talks: How a Medical Manufacturer Revolutionized Their Process with Palletizing What's the buzz all about? ✅ TIDI Products has adopted Robotiq's advanced Palletizing Solution, setting a new standard in automation. ✅ Discover the impressive results of TIDI's automation initiatives, including significant increases in efficiency and worker safety. ✅ Cameron Lemke, Value Stream Manager at TIDI Products, will share his valuable experiences from the front line of automation. Why attend? 🚀 Get insights from those with first-hand experience implementing palletizing automation solutions. 🔍 Dive into the secrets of how TIDI Products have enabled productivity breakthroughs. 🤝 Listen, connect and get answers directly from the industry leaders themselves. Register Now: Tuesday, April 23 @ 10:30 am EST https://lnkd.in/g6Y2v7cj
To view or add a comment, sign in
-
🔊 Our webinar for MED Companies is coming! Be sure to register and don't miss the opportunity to discuss this critical topic: "Achieving Digital Transformation in Medical Device Manufacturing" with Andea, MassMEDIC , and one of Andea's Customers - Straumann Group. #beapartofdiscussion #medicaldevices #webinar #Straumann #Andea #MassMEDIC
Join us on September 12th at 11 am ET for a webinar hosted by Andea, focused on Achieving Digital Transformation in Medical Device Manufacturing. The webinar will cover how to ensure a rapid response, accurate impact assessment, effective product quarantine, and seamless manufacturing adjustments when making digital transformation. Learn more and register here: https://bit.ly/3yzo2fI
To view or add a comment, sign in
-
The increasing use of off-the-shelf (OTS) software in medical devices is driven by the availability of general-purpose hardware. This shift lets manufacturers concentrate on device-specific software, though OTS software might not always meet regulatory requirements. Manufacturers forfeit control over the OTS software lifecycle but remain responsible for ensuring the device's safety and effectiveness. The US FDA has updated guidance "Off-the-shelf (OTS) software in medical devices" to reflect least burdensome approach for necessary documentation for premarket submissions. I’m speaking at "Global Regulation & Software for Medical Devices Digital Week" on 08th Aug, 2024 about recently updated guidance and best practices for “Managing off-the-shelf (OTS) software in medical devices” https://lnkd.in/ghsauVuP
Global Regulation & Software for Medical Devices Digital Week
informaconnect.com
To view or add a comment, sign in
-
🔒 Achieving pharma compliance just got easier with our Track & Trace solutions! 🚀 Our experienced team will guide you every step of the way, from pre-sales to support, ensuring effective implementation. Don't miss our video to learn more! #PharmaCompliance #TrackAndTrace https://okt.to/NdWGwh
Boost your productivity with METTLER TOLEDO smart track and trace solutions
https://www.youtube.com/
To view or add a comment, sign in
-
Streamlining compliance and automating documentation has never been easier! Rapidfacto helps medical device manufacturers focus on what matters. 🚀 Save time and stay compliant with one-click automation. #MedicalDevices #Automation #ISO13485 #MDR
Are you tired of time consuming paperwork slowing down your medical device operations? Rapidfacto makes documentation effortless with one-click BMR generation, 20 automated reports, and ISO 13485/MDR-compliant solutions. 🚀 Our software helps medical device manufacturers: ✅ Save 90% of time spent on documentation ✅ Automate key processes across manufacturing, quality control, and inventory ✅ Stay audit-ready with all records having a built-in audit trail Say goodbye to manual work and embrace automation to scale your business! 💼 👉 Book a free demo today and see how we can transform your documentation processes. Visit www.rapidfacto.com 📞 91 8708856807 ✉️ [email protected] #MedicalDevices #Automation #ISO13485 #QualityControl #Manufacturing #ProcessAutomation #MedicalDeviceCompliance #Rapidfacto
To view or add a comment, sign in
-
📢 Creo Medical Group plc (#CREO) provides a trading update for the year ended 31 December 2023, including an overview of its commercial and clinical progress. 💪 New products support strong growth and accelerate commercial momentum of Creo's core technology 📈 Double digit Group revenue growth and ongoing cost control 💰 The Company expects to report growth in Group revenues of 13%, from £27.2m in FY22 to £30.8m in FY23. ⬆ Core technology sales and Kamaptive licensing income increased to £4.0m (FY22 £2.3m) with core technology sales increasing c. 2.5x. 🗺 Speedboat® UltraSlim has been used successfully in procedures in the UK, USA, LATAM and APAC 🔗 https://lnkd.in/e-EAR2EH
To view or add a comment, sign in
42,733 followers