There’s a multitude of pitfalls to gaining market approval for MedTech products – not all of them obvious. We’re grateful to @The-engineer-uk for sharing Dr Stuart Grant’s insight into recognising and overcoming the hurdles faced by innovators. You can read it here: https://loom.ly/a7sXNr8 #MedTech #marketapproval #innovation
关于我们
Archetype is an innovation management consultancy with unparalleled expertise in obtaining market approval for medical devices. In the MedTech space today, there is no blueprint for success. A constantly changing market creates difficulties at every turn, and it’s never been harder to make something new. Even legacy products now face an uncertain future. In this environment, the already all-consuming question, “Can it be done?” becomes, “Even if it can be done, will it be allowed?”. At the same time, the rewards for success have never been greater. Not just in terms of money, but in terms of the number lives around the world that can be improved. That’s what motivates us. We consider our purpose profound: to grant patients access to the transformative power of cutting-edge medical devices. We seek to empower MedTech entrepreneurs with strategic insights, unwavering support, and the guidance needed to achieve market approval. Because it is only when your product is both functional AND available that it can fulfil its purpose: helping people. That’s why we made our company. Archetype. Making MedTech Success.
- 网站
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www.archetype-medtech.com
Archetype MedTech的外部链接
- 所属行业
- 战略管理服务
- 规模
- 2-10 人
- 类型
- 私人持股
- 创立
- 2023
- 领域
- Innovation Management、Market Approval、Regulatory Pathway Design、Programme Management、New Product Development、Design Control Procedures、Risk Management、Requirements Management、Regulatory Assessment、Expert Technical Reviews、Investor Validation Reporting、Investor Due Diligence、Training、Workshop Facilitation、Medical Devices、Processes & Systems Design、Product Innovation Strategy、Risk Appraisal & Mitigation Strategy、MedTech和Product Innovation Process
Archetype MedTech员工
动态
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Medical Technology UK 2025 provides a unique opportunity for medical device manufacturers to connect with suppliers, and encourages collaboration within the medical device and engineering community. This event is designed to provide tangible industry solutions for all involved. #MedicalTechnology #Innovation #MedicalTechUK #ArchetypeMedTech
Excited to be heading to Medical Technology UK 2025 for the next two days! Looking forward to the insightful sessions, especially the Future of Medical Technology Innovation program led by Karen Taylor and the Disruptive Innovators in MedTech program chaired by Dean Fathers. This event stands out as the UK's premier medical device design, development, and manufacturing event tailored specifically for the UK medical device engineering community. If you'll be attending, it would be great to connect! Let's make the most of this opportunity to meet and network. #MedicalTechUK #ArchetypeMedTech #MedTech #Innovation
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Great to see @MedicalProductOutsourcing sharing this article by Dr Stuart Grant, which identifies the hidden hurdles to gaining MedTech market approval and suggests strategies to overcome them. You can read it here: https://loom.ly/uDfU5QE #MedTech #marketapproval #innovation
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“While MedTech remains a necessity throughout a lifetime, and technology continues to change and advance, one thing remains steady year after year – market growth.” Read Today's Medical Developments Magazine 2025 Forecast to learn insights from throughout the industry regarding the state of medical devices manufacturing and what our Founder & Principal Consultant Stuart Grant and other thought leaders see for 2025. https://lnkd.in/edAu29Yp
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MPO has a few winning stories this week; I especially enjoyed reading about the key considerations with clinical trial sponsors. #MedTech #MedTechInnovation #Archetype
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??PODCAST From Blueprint to Breakthrough: Navigating MedTech Innovation Make sure to catch Archetype founder Dr Stuart Grant with Thomas Hickey on the MedTech Guru podcast. He discusses his 25-year career in MedTech and his mission to support start-ups and entrepreneurs to gain market approval for their innovative medical devices. Tom describes their conversation as: “Brimming with actionable insights" Don't miss out. Listen in and see what you think ??https://loom.ly/-XedJQY #MedTech #MedtechInnovation #MedTechGurus
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LumipenPro is attending the 2025 ABAM meeting in Park City, UT! Booth #24 https://lnkd.in/gMFJkSmc
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??This is worth a read - the World Economic Forum highlights AI’s transformative impact on healthcare, including enhanced diagnostic accuracy, optimised ambulance dispatch, and early disease detection. ??It emphasises the importance of responsible AI implementation to bridge global healthcare gaps, offering a compelling vision for AI-driven medical advancements. Take a look ?? https://loom.ly/irmm3ps
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Thank you to Orthopaedic Product News for featuring our thoughts on the use of ISO 14971 in driving innovation. You can read it here ?? https://loom.ly/rzjSmTY #medicaldevices #drivinginnovation #orthopaedic
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The MedTech industry is just beginning to recover from the impact of the Medical Device Regulation (MDR), which required significant resources to address compliance, but with questionable improvements in patient safety. With that in mind, is now really the right time for the EU to introduce another broad regulation that could further limit EU patients' access to beneficial new devices? This article by @osborneclarke provides a good overview of the new ‘green deal’ for MedTech. See what you think. https://loom.ly/0jwyy8Y