与20,000+医疗器械成品企业共探创新
区别于展出终端成品医疗器械的展会，Medtec 主要面向研发部、工程部、设计部、采购部、工艺部、管理、质量部、法规部的工程师、决策者和各级影响者。为各方提供一个交流多样想法和解决方案的平台。
探索医疗器械研发与生产解决方案
在这里可以自由探索每家展商产品，为贵司提供独一无二的解决方案。2026年9月1日-3日，上海新国际博览中心N1-N4，专属医疗器械生产和研发的品质聚会。
Medical device companies are changing healthcare delivery by using advanced commercial intelligence platforms that track complete patient journeys across providers, diagnoses, and treatments, solving the persistent challenge of murky referral networks.
New data platforms illuminate murky healthcare referral networks, helping medtech companies target education efforts.
Longitudinal patient data transforms referral blind spots into clear pathways for optimal specialized care.
80% of physicians report being overworked, making it crucial for medtech to guide treatment awareness.
Around 90% of manufacturing leaders recognize smart factory initiatives as critical for competitiveness. Siemens Healthineers’ Paavana Sainath discusses how the future healthcare workforce requires multidisciplinary expertise, digital fluency, and virtual development skills
In the age of AI and automation, if industries are not ahead of the curve, they are often falling behind.
According to a May DeDeloitte survey that connected with 600 executives from large manufacturing companies based in the U.S., 90% of manufacturing leaders see smart factory initiatives as critical. Specifically, the integration of advanced automation, real-time data analytics, and AI-driven decision-making.
After significant delay and protocol pivots, the European Database on Medical Devices is poised to officially initiate complete compliance measures officially. How can manufacturers sift through the confusion?
EUDAMED compliance will soon be mandatory for all medical device makers seeking EU market access, not just EU companies.
Delaying EUDAMED registration risks market disruption while early adopters gain competitive advantages.
The system transitions from voluntary to mandatory in early 2026, requiring immediate preparation.
Explore the critical role of electronics cleaning validation in medical device manufacturing. Learn about regulatory requirements, contamination risks, and effective cleaning methods
Vapor degreasing emerges as a superior cleaning method for complex medical electronics, ensuring regulatory compliance.
Proper electronics cleaning validation is critical for patient safety as medical devices become increasingly miniaturized.
Structured IQ/OQ/PQ validation framework essential for medical device manufacturers facing heightened regulatory scrutiny.
The Growing Connectivity Dimensions in Medical Technology
Artificial intelligence (AI), augmented reality (AR), virtual reality (VR), remote treatments, smart wearables, robotic mobility, and automation. Next to the ongoing evolution of evermore precise images and real-time videos, as well as evermore mobile and compact machines, the recent communication megatrends shift medical technology into the next level of healthcare digitalization.
Test and Measurement: Regulatory Updates and Strategic Implications
Medical device companies are operating in a climate of rapid transformation. The traditional regulatory and testing frameworks that have guided development for decades are evolving, prompted by technological innovation, increased globalization, and lessons learned during recent public health challenges.
Fiber Computer Allows Apparel to Run Apps and “Understand” the Wearer
What if the clothes you wear could care for your health? MIT researchers have developed an autonomous programmable computer in the form of an elastic fiber, which could monitor health conditions and physical activity, alerting the wearer to potential health risks in real time.
Wearable Mimics CT Scans, Delivers Continuous Monitoring of Heart, Lungs
Researchers have developed a first-of-its-kind wearable device capable of continuously scanning the lungs and heart of hospital patients while they rest in bed — offering a revolutionary alternative to CT scans.
