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On-prem Topic-based Authoring and Publishing

MadCap Central

Your hub for streamlined content collaboration and management

MadCap IXIA CCMS

Enterprise-class Component Content Management System (CCMS)

MadCap Xyleme LCMS

Enterprise-class Learning Content Management System (LCMS)

Navigating the Complexities of Medical Device Information with MadCap Software


Webinar Summary

Presented By:

photo of Solena Le Moigne, webinar presenter
Solena Le Moigne, Content Architect | Elegance in Chaos

Join us for an enlightening journey through the intricate landscape of medical device documentation and discover how MadCap Software's suite of HATs (Help Authoring Tools) rises to meet the industry's unique challenges.

 We'll embark on our exploration by delving into the critical need for manufacturers to demonstrate their competence, the efficacy of their processes, and the reliability of their partners and providers. Whether you're new to the field or a seasoned expert, we'll demystify the categories of medical devices, outline the journey from conception to clinical use, and discuss the importance of voluntary compliance with industry standards.

As we consider the broader implications of successful medical devices or the integration challenges posed by corporate mergers, we'll reveal how MadCap Software solutions empower departmental autonomy in information management while fostering interdepartmental collaboration to satisfy QARA regulations.

 This webinar isn't just a presentation; it's an invitation to challenge the status quo, to question and refine your understanding, and to equip yourself with the knowledge and tools necessary for excellence in medical device documentation.

Secure your spot now and be part of the conversation that's shaping the future of medical device information management with MadCap Software and Elegance In Chaos.

 Key Highlights:

  • An introduction to ISO 13485 and its significance in establishing a Quality Management System.
  • A look into how MadCap Flare not only helps to meet validation requirements but also enhances coherence and traceability in documentation.
  • Insights into the necessity of robust document creation processes.
  • Strategies for leveraging a single repository to generate diverse file formats essential for regulatory compliance, such as MDR and IMDRF.
  • Techniques for managing translations effectively to fulfil legal obligations.
  • Approaches to versioning and traceability – can a CCMS streamline the process?

Secure your spot now and be part of the conversation that's shaping the future of medical device information management with MadCap Software and Elegance In Chaos.