Medical Device Innovation Consortium (MDIC)

Discover key milestones from MDIC’s 2024 Year in Review in this special edition of SIGHTLINE! Highlights include: •     Insights from #APF2024, showcasing equitable innovations in women’s health. •     Key takeaways from the Patient Summit on the transformative impact of Patient Preference Information (#PPI). •     Breakthrough advancements in advanced manufacturing, including 3D printing and #AI adoption. •     Top MDIC stories, such as trending topics in MedTech for 2025, MDIC's #CRISPR milestone, and most-watched videos from 2024. Dive into these updates and more to see how MDIC continues to drive quality, innovation, and collaboration across the MedTech ecosystem. 📩 Not receiving SIGHTLINE yet? Sign up today: https://lnkd.in/gHkxD9vV

2024 has been a pivotal year for medical device innovation, with #APF2024 sparking critical conversations about women's healthcare. Visionaries including Cat Bohannon and Dr. Renee Wegrzyn pushed the boundaries of conventional thinking, showing how breaking free from male-centric approaches can lead to more inclusive and impactful care for women. The insights shared at this event are paving the way for a more inclusive and innovative future in healthcare. Explore the key moments and ideas that are redefining what’s possible: https://lnkd.in/ePqkj4tz #WomensHealth #MedTech #HealthcareInnovation #MDIC

There’s still time to participate in the Annual MDIC Medical Device Cybersecurity Maturity Industry Benchmarking assessment. We have extended the survey to January 17th. This free, online tool evaluates your cybersecurity posture against established industry rubrics and provides actionable insights. Why Participate? -Instantly receive a report highlighting potential vulnerabilities and areas for improvement. -Benchmark your performance against industry peers. -Gain insights to strengthen cybersecurity across your product life cycle. Developed in collaboration with Health Sector Coordinating Council - Cybersecurity and Apraciti, this assessment is your opportunity to enhance device security while contributing to industry-wide improvements. Don’t miss out—help build a more secure future for medical devices! Take the assessment before January 17th: https://lnkd.in/ePXrGT3a #Cybersecurity #MedicalDevices #benchmarksurvey

How can the patient voice lead to better patient outcomes and more meaningful solutions in #MedTech? Our latest Quick Takes, Key Insights video highlights why Patient Preference Information is critical in regulatory and payer decision-making and shares insights from experts in this field, Barry Liden and Juan Marcos González Sepúlveda. By understanding and prioritizing #patientpreferences, we can better ensure that medical technologies align with patient needs, ultimately improving access and care. #PatientVoice #PatientSafety #MedicalDevices #Reimbursement #HealthInsurance #PatientInput #PatientAdvocacy Watch now: https://lnkd.in/ezkBbNxn

Join us next Thursday December 12th at 11am ET for an insightful webinar in our Regulatory Applications in Computational Modeling & Simulation series. Cook Medical and Dynatek Labs will reveal a groundbreaking method for cardiovascular device testing. Learn how their innovative benchtop testing approach uses finite-element analysis (FEA) to predict real-world outcomes, supporting safer and more effective medical device development. Secure your spot and explore how computational modeling is transforming MedTech innovation. Register Now: https://lnkd.in/gtUBWJ7w Presented by: Boudreaux, Ph.D. Ray and Zhao Xuefeng

Four of MDIC's program directors sat down with Clinical Leader to discuss trends shaping the future of #MedTech innovation. From Science of Patient Input and Clinical Diagnostics to IVD Standards and Early Feasibility Studies, this conversation sheds light on the collaborative efforts driving meaningful progress in medical device and diagnostic development. Explore insights from Kert G., Maryellen de Mars, Pipper White, MSc, PMP, CCE(r), and Eileen (McDonald) Mihas, RN, MSN-HSL on how their programs are driving MDIC’s mission to improve #patientoutcomes and enhance regulatory science. Read the full article: https://lnkd.in/ep_aPF6T #MDIC #MedTechInnovation #MedicalDevices #Diagnostics #HealthcareInnovation

The MDIC Annual Patient Summit showcased powerful discussions on Patient Preference Information (PPI) and its impact on medical device development. Patients, caregivers, and researchers highlighted how PPI can reshape clinical trials, device design, and healthcare solutions by aligning with what patients truly value. Watch the full session to explore how patient insights are leading to a more patient-centered future in healthcare. Watch Now: https://lnkd.in/dq_7nrEG

Discover How Real-World Evidence is Transforming MedTech! Learn NEST's critical role in catalyzing the use of #RWE to streamline submissions, accelerate time-to-market, and lower costs for #MedTech companies. With a focus on post-market data, off-label use, and pivotal test cases like pediatric devices and robotic surgery, this conversation reveals the immense potential of RWE to improve patient outcomes and advance medical innovation. Listen Now: https://lnkd.in/d7n5BzaM

Join us December 12 at 11:00 AM ET for a case study webinar on an in silico testing method capable of intentionally fracturing nitinol stents in a controlled, pulsatile environment. This groundbreaking approach allows researchers to validate predictions from finite-element analysis (FEA), accurately pinpointing where fractures are likely to occur and the conditions that trigger them. Speakers, Dr. Ray Boudreaux and Dr. Xuefeng Zhao, will demonstrate how computational modeling and simulation can enhance the accuracy of stent testing and offer practical insights into how FEA can predict real-world outcomes, supporting safer and more effective #medicaldevice development. Register now: https://lnkd.in/e5TdQzmv Zhao Xuefeng | Boudreaux, Ph.D. Ray #computationalmodeling #insilico #clinicaltrials #medicaldeviceapproval #medtech #regulatory #FDAsubmission #healthtech

Michelle Tarver, MD, PhD has officially stepped into her role as Director of the FDA’s Center for Devices and Radiological Health (CDRH). While challenges lie ahead, both patient groups and industry leaders remain optimistic about her ability to lead with vision and collaboration. Dr. Tarver’s extensive experience and commitment to patient-centric initiatives signal exciting opportunities for innovation and progress in medical device regulation. Read more about how her leadership is shaping expectations across the MedTech landscape: https://lnkd.in/guRH-c8j (MedTech Dive)