Florida Medical Manufacturers Consortium’s Post

#2024 has been a record year for #MedTech #M&A MedWorld Advisors ! WIth the Fed about to reduce interest rates (not investment advice - just speculation), it appears that #mergersandacquisitions activity in our industry will only continue to get stronger in the coming months! And if a certain administration wins the election and you are thinking about selling, it may be important to realize your gains sooner than later! Either way, with all the #Strategic M&A and #Drypowder from #Privateequity, it remains a great time to consider selling your #medtech #medicaldevice #digitalhealth #diagnostics #lifesciences #CDMO #CMO #dentaltech business. Florence Joffroy-Black CMAA and myself (Dave Sheppard, CMAA ) look forward to discussing these dynamics and more ! Please take time to join us by registering at the link below! ANd if you can’t make it, please register anyway to gain an access to the recording ! Cheers! Jim Fidacaro Eric S. Heinz Wissam Abousleiman Ryan⭐ Stellar Tom Wilmering Jeremy Thomas MBA Florence Henry-Leroux Estelle Black Rani Shifron 施逢霖 Michael Gentile

There are just over two months to go until the 11th annual American Medical Device Summit comes to Chicago! The Summit gathers 200+ industry leaders as a platform to explore where medical device meets opportunity. We are excited to share one of our esteemed emcee's: Juan Daccach MD, VP, Global Product Safety at Merz Aesthetics. Join Juan and explore strategies for product development and design, optimizing regulatory strategies, managing costs, and more! Discover more summit details here: https://hubs.ly/Q02HP3Xp0 -- #GenerisAMD #MedDeviceUS24 #MedicalDevice #MedDevice #QualityandRegulatory #Clinical #Quality #Regulatory

Today marks the first day of the medical Industry Scientific Exchange (ISE) for new sterilization modalities, hosted in Munich by TÜV SÜD . This event brings together over 75 participants from over 30 medical device manufacturers, sterilization providers, FDA and TÜV SÜD. These experts will have a scientific exchange of ideas on how to address challenges to packaging, biocompatibility, and material science for new sterilization modalities. The presentations and exchange so far has been very enlightening. Looking forward to what the next 3 days bring as experts exchange ideas on bringing these new sterilization technologies forward. #tuvsud #FDA #medicaldevices #sterilization

A day full of engaging content at the AboutMedicalDevices conference, organized by AboutPharma . The event featured a panel of distinguished speakers from the Italian and European regulatory and industrial sectors. In the Italian medical devices industry, which currently includes 4,640 companies and 117,600 employees, a concerning trend has emerged: investments in research and development have dropped by 30%. Is this a temporary and structural issue? It is evident that regulations have made Europe a less attractive market compared to other countries, such as the United States, where regulations are less stringent. Today, Europe is the last region where innovations are launched. To close this gap, it is essential to regain a comprehensive vision of the process from design to production and marketing of medical devices. This was highlighted by the vice president of Confindustria medical devices. His speech reflected an awareness of the national industry's limitations and the challenges of competing in an increasingly competitive market. Aglatech14 S.r.l. #AboutMedicalDevices

The introduction of the ICMED 13485 Plus scheme is seen as a game changer for the Indian MedTech Industry. The innovative scheme marks a significant milestone in ensuring the quality, safety, and efficacy of medical devices. By integrating Quality Management System components and product-related quality validation processes, ICMED 13485 Plus sets a global benchmark in the industry. #ICMED_13485_Plus #scheme #MedTech #industry #quality #validation

Very insightful ! Read about: - Pyrogens, Alternative Methods: Monocyte Activation Test - Questions from Notified Bodies: how to answer them? - Usability Techniques for Compliance: the use of Annex C of IEC 62366 - Planning an implantation study to evaluate local tissue effects - Special Hemocompatibility Testing: Considerations for testing transfusion equipment sets according to ISO 1135-4/-5

Are Medical Device Suppliers Equipped for the Escalating Regulatory Landscape? The global medical devices market is projected to surpass $886 billion by 2032. As these devices become increasingly critical to patient outcomes, regulators are tightening their quality and safety expectations. But how well prepared are suppliers to meet these rising standards? We recently commissioned independent research to find out. The 2024 study surveyed 202 regulatory professionals at Class 2 and 3 medical device companies in Germany and the US. The findings highlight several key challenges and assess the current state of regulatory readiness among device suppliers. Read the article here: https://lnkd.in/ezWnaknB

Stay informed about FDA updates to the Breakthrough Devices Program by checking out our latest blog post! This Program helps expedite development and review of eligible medical devices while ensuring their safety and efficacy. Take a look at our helpful breakdown of how devices might qualify for this pathway.  Healthcare Innovators - is this program right for your technology? BMTA can assist you in navigating this and other potential paths in the evolving landscape of medical device regulation. #BMTA #FDA #BreakthroughDevices #MedicalDevices #HealthcareInnovation #TechRegulation

Did you miss our recent live webinar? Watch our on-demand webinar, "Navigating Innovation: Deep Dive into Opportunities and Challenges within the Regulatory Landscape," presented by TÜV SÜD in collaboration with Qserve Group. 🔍 In this comprehensive program, we explored the future of medical devices across four crucial topics: 1. Innovative Medical Devices 2. Testing for Device Safety & Compliance 3. MDR Transitional Period 4. Annex XVI Moderated by Dr Andrea Pietsch, our expert speakers, Dr Royth von Hahn and Dr Gert Bos, shared invaluable insights, expertise, and a deep dive into the regulatory intricacies shaping the dynamic landscape of the medical device industry. 📍 On-demand webinar link: https://lnkd.in/egHBzFj8 Stay at the forefront of innovation and regulatory trends! #TUVSUD #MDR #MedTech #Innovation #AnnexXVI #Webinar

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