DESIGN EXCELLENCE FOR MEDICAL DEVICES
Compliant and competitive
Remove paper-intensive workflows – enhance the availability of compliance data and reduce the time it takes to access that data from months to seconds.
As medical device regulations evolve to demand greater control, visibility, accountability and traceability, companies that make orthopaedic and dental devices have no choice but to work smarter.
Compliance is much easier to achieve when manufacturers move away from manual processes and adopt a holistic digital design platform. This forward-thinking approach enables people from across departments to create, manage, share and trace documents.
As well as improving organisational collaboration and improving safety, this single source of information can help get products to market faster by reducing approval wait times.
Navigating regulatory complexity is far from a box-ticking exercise; when you take an integrated approach to data-management, you can stay ahead of growing regulatory scrutiny and boost your competitive advantage.
By dramatically enhancing the availability of compliance data, Wright Medical Technology, Inc, has reduced design approval time from days to hours.
Downloads
To discover what a renewed, holistic focus on design excellence could mean for your business, download our executive brief now.
Executive brief
The business benefits of collaborative design to navigate regulation. Siloed teams working on complex medical device design lead to delays. Learn how Siemens drives efficiency in the creation of safe, effective medical devices.