PTC Blog: Embrace Industrial Digital Transformation

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MedTech leaders recently gathered in Boston to talk regulatory complexity, connected quality, and AI at scale.  

While most medical devices are excluded from the EU Cyber Resilience Act, the regulation signals rising expectations for lifecycle cybersecurity, traceability, vulnerability management, and compliance across MedTech.

PTC and osapiens partner to connect PLM and UDI systems, helping medical device firms meet global regulatory and EUDAMED requirements.

Discover how AI diagnostics, wearable health tech, personalized medicine, and medical robotics are set to revolutionize healthcare. Stay ahead of the curve and explore the future of medical technology with us. #MedTech #HealthcareInnovation #AI #WearableTech #PersonalizedMedicine #MedicalRobotics"

Break down NPI barriers in MedTech. Learn how leading manufacturers reduce design control cycle time while accelerating innovation, compliance, and patient safety.

Cybersecurity is a rising concern in the MedTech industry. The Omnibus Bill addresses this concern. Find out how the bill affects medical device OEMs from our blog!

A QMS is a system of policies and procedures ensuring medical devices meet safety, quality, and regulatory standards throughout their lifecycle.

What is CAPA? Find out more about the importance of corrective and preventative action in manufacturing.

Discover how PLM, ALM, and SLM help MedTech companies adapt to tariffs and maintain compliance.