Joe Mullings’ Post

After a bumpy last five years, the US Medical Device Manufacturing industry is poised for new growth driven primarily by increased investment and technological innovation. 💡 In a recent article they wrote for Expansion Solutions magazine, our Senior Vice President Jim Damicis, Director of Workforce and Industry Alexandra Tranmer, CEcD, and Analyst Dawn Otterby took a closer look at the latest data on Medical Device Manufacturing trends, forecasts, and investments and explained how economic developers can take advantage of emerging opportunities within this industry. Read it here 👉 https://lnkd.in/g3Ac8tVD #manufacturing #medicaldevices #economicdevelopment

With a less than 12% probability of clinical success for medical devices in the market, it's clear something in the legacy design and development process is broken. These gaps are leading to delays in project timelines, costly rework, and designs that fall flat in the market. Most in the industry are at the point of accepting these risks, the costs, and the timelines without question.   But, there is an alternative option that MedTech OEMs have when designing, developing, and manufacturing medical devices.   At MPE Inc., we've purpose-built the new pathway to capital equipment commercialization with a customer-centric, unified approach to product design, development, and manufacturing. Our MedTech experts are ready to support you when and where you need it. Leave the legacy pathway behind and learn more here:   https://lnkd.in/g9hch6Ar   #mpe #medtech #medicaldevice

Dear network, as mentioned in our post from today, I'll be more than happy to receive your message, to discuss those topics further 😀 #sanner #sannergroup #medicaldevice #medicaltechnology #medtech

🔬 Exciting news! Debiotech SA experts share with you the crucial role of systems engineering in medical device development. 💡 Find out how this interdisciplinary approach guarantees efficiency, safety and innovation in our latest article! 🚀 Dive in now 👇 #SystemsEngineering #MedicalDevices #ServiceProvider #DebiotechExperts 

As we look back on the past 25 years at Natech, the journey has been nothing short of remarkable. From growing teams to expanding services for medical and diagnostics devices, we've seen our organization evolve exponentially. The growth is not just in numbers but in capabilities, collaborations, and community. Each year that we expand, the significance of what we do also grows. Every innovation, every project, and every milestone matter more than ever. For us, progress isn't just about moving forward; it's about making an impact. #NatechGrowth #25YearsStrong #Evolution #Community #InnovationMatters #Milestones #Team #MedicalDevices #Diagnostics #Consumables #InjectionMolding #ContractManufacturing

I speak for all three of us (Karl Lindborg CEO, Owner, CPO LP, Susi Ebersbach, and myself) when I say, we hope you enjoy this article and find it helpful and useful. Thank you to the The O&P EDGE for publishing this great issue and to Karl Lindborg CEO, Owner, CPO LP for giving me the opportunity to contribute. Thank you also to all the manufacturers for helping me compile this information. Össur, Ottobock, Open Bionics, PSYONIC, Aether Biomedical, BionIT Labs, COVVI Please reach out if you have ANY questions at all. Article link 👉 https://lnkd.in/ey_xJrAN P.S. More about this article coming on my business page, Calibration Marketing - Achieving Marketing Outcomes in O&P. #oandp #prosthetics #prosthetichand #bionichand #upperlimbprosthetics #amputee #handamputee #marketmanagement #productmanagement #productmarketing

Developing a new medical device - for a drug delivery, diagnostic, or medtech application – with speed and efficiency, means shorter time to market and a healthier bottom line. This is a valuable prize, so, how do you win it? This post is the first in a series in which we’re going to look at different tools and strategies for device development and their merit, though the lens of our experience here at Sanner. Good Design for Manufacture and Assembly (DFMA) is a great philosophy for device development. This engineering methodology calls for the consideration of factors that influence the manufacturing and assembly of a device right from the outset of the development process. And we have the digital tools and software to help you apply it. Digital twins, rapid prototyping and virtual reality are all elements of the DFMA toolkit that we apply to help you to determine as early as possible whether a design can be manufactured, and more generally, reduce the risk and development time associated with bringing new devices to market. If you like to discuss this further please contact Markus Roitzheim. Read more about how to speed your device development project to success: CDMO Insights: https://lnkd.in/eWHRVYfJ. #sanner #sannergroup #medicaldevice #medicaltechnology #medtech

Learn how an accomplished medical device engineer overcame challenges in manufacturing processes and navigated tough regulatory hurdles. Listen to this episode with Dion Lopes as he shares invaluable insights on welding nitinol wire, optimizing processes, and accelerating engineering.

What are the benefits of using the system engineering approach during the development of your medical device? See the post below 👇

Finding the right balance between efficiency and flexibility can be a game-changer in medical device development. As innovators bring cutting-edge products to market, they often face the challenge of optimizing production processes while maintaining the agility to adapt to changing needs. At Meddux, we've seen firsthand how mastering this balancing act can make all the difference. Our experience has taught us that the key lies in developing custom manufacturing processes that are robust and scalable and tailored to each product's unique requirements. We've found that implementing Design For Manufacturability (DFM) strategies early in the development process is crucial. By anticipating and addressing potential production challenges upfront, we can reduce costs and improve efficiency as products scale up. But efficiency alone isn't enough. Flexibility is equally essential in an industry where time to market is critical. Being able to respond quickly to changing demands, whether ramping up production for a clinical trial or pivoting to address a new market opportunity, can be the difference between success and missed chances. So, how do we achieve this balance? It starts with a continuous improvement mindset, a focus on quality, and a willingness to think outside the box. It requires a team of skilled engineers who can troubleshoot problems and proactively identify optimization opportunities. While balancing efficiency and flexibility is a continuous journey, the potential rewards are substantial. Those who can navigate this balancing act can look forward to accelerated time to market, reduced costs, and the ability to bring life-changing innovations to patients faster. Want to optimize your production processes and accelerate time to market? Partner with Meddux and experience the power of efficiency and flexibility. Find out more at https://meddux.com/. #Meddux #MedicalDeviceDevelopment #MedicalProductDevelopment #CustomProcessDevelopment #ContractManufacturing