SAI Global has global experience in providing Standards, technical information and regulations. We bring this content together in a software solution that enables Medical Device organisations to stay compliant, manage risk, boost productivity and gain a competitive edge in an environment where being on top of your game is critical to saving and extending lives.
Centralise your internal and external information
- Simplify the manual compilation of lists and tasks - notes and bookmarks in one place
- Reduce the maze confusion of different licensing models - all your Standards housed in one repository for all of your team to access
- One hub, one invoice, one frame of reference - thousands of Standards
Rely on current information to improve proactivity and efficiency
- Get notified when Standards change
- Readily accessible audit list of changed, amended and superseded Standards
- View new and old Standards side by side
- Make sure everyone is relying on the right content, always
Gain the context needed for each medical device under development
- Create and manage project folders of content specific to each product being worked on
- Share Standards with everyone including remote members of the team
- Link to relevant internal and external documents and integrate with your product workflow
Take back control of your budget, copyright and content management
- No duplicate purchases as only designated users have permission to purchase
- Know that no user will be using different versions of the same Standard
- Strict document management provided by us to assist in avoiding copyright abuse
Which functions will benefit from a robust Standards Management Strategy?
- Production and Manufacturing
- Regulatory and Legal Affairs
- Product Design Engineering
- Research and Development