Are you ready to share your story of digital transformation? Join Joseph Sapiente, Vice President of Clinical Science and Technology at MDIC, and Francisco Vicenty, Program Manager for Case for Quality at the FDA, as they discuss the evolution of the Advanced Manufacturing Clearing House initiative at MDIC and how you can get involved: https://lnkd.in/eU-TEVFt #medtech #digitaltransformation #medicaldevices #FDAapprocal #AMCH #advancedmanufacturing #innovation #patientsafety
Medical Device Innovation Consortium (MDIC)’s Post
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The countdown to #medTechCon is finally over! Make sure to visit the Hydrix team at Booth 720 to discover how our drag and drop strategy can rapidly resolve your product innovation challenges. #innovation #medtechcon #MedTechCon #AdvaMed #medicaldevices #uidesign #marketinsights
Medical Device Development | ISO 13485 | Hydrix
https://www.hydrix.com
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The #medtech market is very likely to grow over the next few years, and #additivemanufacturing will play a big part. In this article, my colleague Benjamin shares some must-read advice about taking advantage of that growth while ensuring your #qualitymanagement is up to standard. #materialisemanufacturing #innovation #technology
AM for Medtech: Building a Quality Management Ecosystem
social.materialise.com
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Clinical phase technology transfer While most discussions are around the transfer to commercial scale manufacturing, it should be remembered that process and assay information (tech) transfer also occurs at all points through a products life cycle from development to production end of life, including through the clinical trial phases. My latest memo looks at the technology transfer at the clinical trial stages. https://lnkd.in/gBFn72pu
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Returning to sharing his thoughts on the use of automation in medical device manufacturing is Ethan Bruyn, manufacturing technology leader at Medbio, LLC. In this Q&A, he addresses one of the most favorable aspects of using automation and also shares questions he gets from medical device firms. #Automation #MedicalDeviceManufacturing https://bit.ly/44rC2mj
Automation for Medical Device Manufacturing Revisited—MPO Videobites
mpo-mag.com
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Medical devices continue to shrink in physical size, while becoming increasingly more complex. In compact drug delivery devices, reliability and usability are paramount. But the physical form and performance of components can be altered drastically with a change in size. When patient outcome trumps all other requirements, wire shaping and forming experts are necessary in ensuring performance and reliability still meet industry standards. Advanex Medical have industry-leading engineering experts with decades of combined experience to provide innovation and reliability to every project we undertake. To find out more, click on the blog post in the comments below 👇
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In this insightful blog post, Surendiran sheds light on the challenges faced by medical device manufacturers and how solutions from Dassault Systèmes help them in overcoming these challenges which would in turn accelerate the product development process, enhance innovation, and deliver products in compliance with regulatory norms and patient-centric approach. Read more: https://lnkd.in/gPT3iFX3 #medicaldevices #simulation #productdevelopment #healthcare
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Accelerate Your Medical Device Journey Without Compromising Quality 🚀 Whether you're in early development stage or gearing up for manufacturing, our seasoned team is here to guide you every step of the way. What sets us apart? ✅ Material knowledge: Deep-rooted expertise in flexible materials including films, foams, and plastics. ✅ Comprehensive capabilities: From design and rapid prototyping to high volume production. ✅ Partnership: An extension of your R&D and engineering teams - supporting startups and OEMs alike. ✅ Pre-Production Validation: Our robust Quality Management System mitigates risks ensuring smooth transition from prototype to production. ✅ Quick turnaround: We're speed to market and outcome-focused. Wherever you are in your product's journey, UFP MedTech provides key areas of support. Visit us at MD&M West Feb. 6-8 at booth #2313 to discover how we can elevate your next project or connect with us at: https://bit.ly/3HvBBgO #MedTech #MedicalDevices #RoboticSurgery #SterilePackaging #MDMWest #IMEWest Informa Markets
Contact Us - Medical Solutions by UFP MedTech
https://ufpmedtech.com
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Truly interesting discussion how to accelerate adoption as well awareness of advanced manufacturing technologies in medical devices industry. How to get from product compliancy to quality,break barriers between requlators and companies and help whole industry ecosystem to implement NG of manufacturing💪.
Join industry leaders Domhnall Carroll, CEO of Digital Manufacturing Ireland, Garth Conrad, Vice President of Quality at Flex Health Solutions, Daniel Matlis, CEO and Founder of Axendia, Inc., and Francisco Vicenty, Case for Quality Program Manager at the FDA CDRH, in a compelling discussion on the adoption of #advancedmanufacturing in the #medicaldevice field. Discover how companies are tackling barriers such as ROI and internal expertise, common fears and misconceptions industry has on advanced manufacturing, and how regulatory agencies are evolving their approach. Watch now: https://lnkd.in/eM9pFrxx Learn more about MDIC's Advanced Manufacturing Clearing House: https://lnkd.in/eTW4YD-d
MDIC Studio Panel: Challenges to Adopting Advanced Manufacturing in MedTech
https://vimeo.com/
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You've seen our 2023 Boston Innovation winners – now it's time for our 2023 Silicon Valley Innovation Showcase winners. First up is the People Choice Award. Eagle Medical Inc, Sterilization, Inc. took the honor with their PATH (Packaging Accelerated Timeline Help) product. PATH True-Validated packaging compresses timelines by eliminating the need to design and build packaging, source materials, validate processes, and test the packaging. The system includes both inner and outer sterile barriers (suitable for implants) along with a single-pack product box and labeling. Additionally, PATH participants receive a complete representative data set backed by reports, charts, and protocols based on actual distribution testing after sterilization, which allows easy adoption of the packaging and process into any QMS. The sole remaining task is to write up the adoption rationale and submit it to the FDA. The resulting contraction in launch schedule equates to $250,000 to $1 million in average burn-rate savings and can provide the competitive edge required to win the race to market.
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Learn how gener8 is leveraging Hawk Ridge Systems solutions to transform the medical device manufacturing landscape with data-driven innovations. Join the conversation on The Engineering Roundtable! https://bit.ly/3SHZect #MedicalDevice #Innovation #DataDrivenInsights
Medical device design and production: using data to advance the state of the art
engineering.com
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