meddevo eTD

Document Management & eSignature Tools

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Meddevo offers a thorough solution for automating technical documentation and managing regulatory affairs in the medical technology industry. Features designed to streamline processes and reduce workload, it supports over 60,000 medical devices, making compliance easier and more efficient.

meddevo eTD can be found in Document Management & eSignature Tools categories.

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Details

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• detects outdated documents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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Technologies Used

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