User Guides
Accessing the System
Transmitting or Uploading Cases to OnePacs
Viewing Cases
Sharing Cases
Reporting Cases
- Proofreading-based workflow ("Review workflow")
- Peer Review
- Result Coding Schemes
- Report Editor Tokens
- Report keyboard shortcuts
Miscellaneous Features
Administrator's Guides
Installation Guides
- OnePacs Desktop for macOS installation guide ( Microsoft Windows
- diagnostic viewer)
- Study Retriever
Administrative Guides
User Management
Workflow Management
Other Administrative Features
Transmission Computer (OnePacs Gateway) Management
- OnePacs Gateway User Interface
- Configuring the Gateway for Direct Downloads
- Configuring Compression
- Configuring the Gateway to route studies to more destinations
- Changing the AE Title of the Gateway
- Configuring the Gateway for Multiple Facilities
- Administrative Interface
Interfacing with Other Systems
FAQ
Support
OnePacs User Forums
Miscellaneous
Certifications and Registrations
According to US Food and Drug Administration classification rules, the OnePacs system is a 'Medical Image Communication Device', or a class I medical device. OnePacs satisfies the requirements of the FDA for manufacturers of Class I devices, including Establishment Registration, Device Listing, U.S. Agent and Quality Systems (QS) regulation (21 CFR Part 820).
According to the guidelines stated in Directive 93/42/EEC of the European Community, the OnePacs system is a Class I Medical Device. OnePacs satisfies the requirements for bearing the CE mark on its labeling.
We self-certify compliance with: