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EU MDR Has Replaced the Medical Devices Directive (MDD) Stay updated on EU Medical Device Regulation (MDR) and the significant changes it brings to the medical device industry with this comprehensive guide.
Ensure Your Medtech Products Meet Customer and Regulatory Requirements This essential guide provides a step-by-step approach to navigating ISO 13485 and implementing a quality management system for medical devices.
Streamline Compliance Audits for ISO 13485:2016 and FDA Title 21 CFR Part 820 Streamline your medical audit and CAPA processes with this comprehensive template to ensure compliance and improve quality in your medtech organization.
Software Design and Engineering Processes through to Validation This comprehensive and easy-to-use template covers all aspects of the medical software engineering process that complies with healthcare regulations.
Top 5 Misconceptions About Remote Condition Monitoring For Medical Device Innovators Don’t let these common remote condition monitoring misconceptions delay valuable, actionable device insights.
Xylem Developing Innovative Solutions to Tackle the World’s Water Challenges Learn how Xylem improves their field service productivity and efficiencies by using ServiceMax, Field Service Management.
A Breakthrough in Custom Medical Implants  
Integrated Customer Data Drives Efficiency at Solta Medical Since implementing ServiceMax, Solta Medical has moved off two legacy systems and unified their customer and product information into one space.
Medical Microinstruments Driving Biomedical Innovation & Excellent Service Medical Microinstruments (MMI) has gone live with ServiceMax to maximize uptime and provide an excellent customer experience.
Aish Technologies  

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