Working with data stored in multiple locations can be time-consuming, costly and risky. By gathering and integrating internal and external critical data to a single location, STEP lets you:
Ensuring information accuracy is critical to meeting compliance requirements. With STEP you can develop complex information management processes and produce necessary documentation by:
In the event of major issues, such as announcing product recalls, having access to fast and accurate information is critical. STEP allows you to handle these events by:
STEP provides you with necessary visibility, from suppliers to finished and delivered products in the hands of your customers.
Compliance issues are currently a huge concern within the medical device market. This White Paper explores the new compliance and regulation landscape, as well as offering some future gazing on what may lie ahead.
Learn how you as a Medical Device manufacturer can comply with these regulations through MDM
How to track devices from manufacture to disposal, and adapt to new business models and technologies
Get a quick one-page summary of how STEP helps you becoming UDI compliant