PTC has solidified its leadership position in the global MedTech market, a critical driver of economic growth and healthcare advancement. At the various MedTech Exchange´s, PTC showcased its commitment to innovation through thought-provoking presentations on "Digital Transformation in MedTech," "Leveraging AI for Regulatory Compliance," and "Innovative Strategies for Cost Management." These events underscored Germany's and North America´s leading role in the global MedTech industry and highlighted the importance of staying ahead in a highly competitive and regulated environment. The insights and strategies shared are set to have a lasting impact on the MedTech landscape, promoting excellence and innovation in patient care.
Who´s Driving Innovation in MedTech?
Discover how top MedTech companies—like Medtronic—are pushing boundaries with breakthrough technologies and forward-thinking strategies. Get inspired by real-world examples of innovation, and learn from the challenges and wins shaping the future of the industry.
Operational Efficiency for MedTech Manufacturing
A strategic guide to improving operational efficiency and cutting costs.
Advancing Life Sciences with PTC ThingWorx: Intelligent, Connected, and GxP Compliant Operations
Discover the power of PTC ThingWorx for connected, GxP compliant, and intelligent regulated-environment operations.
Key requirements for digital transformation in MedTech
Discover essential criteria for selecting a PLM solution to support your MedTech digital thread initiatives. Learn about streamlining engineering, business value, and benefit from implementation tips.
EU MDR: navigating standards for MedTech developers
EU MDR sets higher safety and performance standards for MedTech. Ensure compliance to access the EU market, monitor device performance, and manage risks effectively.
Streamline medical audits and CAPA with Codebeamer template
Effortlessly manage compliance audits and CAPA with our preconfigured template. Access best practices, ensure regulatory compliance, and minimize risks in MedTech development.
Medical Software Engineering Template
This Medical Software Engineering Template consolidates the medical device software design and engineering process, ensuring compliance, efficiency, and quality.
AI for Service | ServiceMax
Harness AI in field service to enhance customer experiences, boost productivity, and add intelligence to operations.
ISO 13485 Medical Devices Quality Management
ISO 13485, the regulatory standard for MedTech Quality Management Systems, emphasizes the importance for medical device manufacturers to develop high-quality products.
MedTech Compliance Technology Handbook
A digital-first guide to streamlining regulatory compliance, reducing risk, and accelerating market access.
7 Forces Driving Up MedTech Costs—What Leaders Must Know
Explore the key cost drivers in MedTech from regulatory complexity to supply chain disruption.
