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meddevo eTD Main Features

• Quality Sync
  You can manage changes and complaints directly in the system, keeping everything in sync.
• RegulatoryAI
  This feature uses artificial intelligence to help you write and manage your technical documents.
• eTD Workflow
  It provides a complete process from data collection to submission, ensuring no data is wasted.
• Large User Community
  Join over 60,000 users who manage their medical devices with meddevo eTD.
• Intelligent Documents
  Documents can automatically update and include data, making your work easier.
• Easy Document Migration
  You can easily import your documents from Excel and start working right away.
• Automated GAP Assessments
  The system can automatically check for gaps in your documentation.
• Audit & Submission Management
  You can track changes and see the difference between submitted and current documents.
• Customizable Approval Workflows
  You can set up workflows that fit your needs for document approval.
• Automated Technical Documentation
  meddevo helps you reduce your regulatory work by more than 50% by automating technical documents.

meddevo eTD Benefits

• saves time
  The system automates many tasks, which helps you save time and focus on more important work.
• improves productivity
  Using RegulatoryAI boosts your productivity by helping with medical writing and managing documents.
• tracks submission dates
  You can easily track important dates and see changes in your documents, helping you stay organized.
• syncs quality management
  The system connects your quality management with technical documentation, making processes smoother.
• reduces regulatory burden
  meddevo helps you cut your regulatory burden by more than 50% by automating technical documentation.
• automates document updates
  It automatically updates documents, so you always have the latest information without extra work.
• detects outdated documents
  It helps you find old documents quickly, so you can keep everything up to date.
• offers customizable workflows
  You can set up approval workflows that fit your needs, making the process more efficient.
• provides a single source of truth
  The system keeps all your data in one place, reducing mistakes and making it easier to find information.

Who should use meddevo eTD?

• Consultants
  They can use the platform to help their clients with regulatory affairs and documentation needs.
• Medical Writers
  They can benefit from AI tools that help create and manage technical documents easily.
• C-Level Executives
  They can make better decisions faster by having all regulatory data in one place.
• Medical Device Companies
  They can manage their regulatory submissions better and keep their documents up to date.
• Quality Management Teams
  They can sync their quality processes with documentation to improve efficiency and insights.
• Regulatory Affairs Professionals
  They can save time and reduce their workload by automating technical documentation.

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