Benefit from a Holistic Strategy to Achieve UDI Compliance!
In this blog post I would like to recommend you to watch the webcast from SAP and p36 on how life science organizations can develop a global strategy to centrally manage UDI product data through automation.
Evolving regulatory requirements are one of the crucial challenges for medical device company’s. Complying and keeping up with UDI regulatory requirements is a very daunting and challenging task, but necessary to ensure your company maintains its presence in current UDI markets, as well as it gives you the opportunity to be prepared for upcoming, unknown regulations.
To keep up, it’s critical to develop a company-wide and global strategy for centrally managing UDI product data using process automation to achieve and ensure global UDI compliance.
But how do you maintain compliance for your company while adopting new business models that are more patientcentric and service-based?
As UDI compliance becomes more complex, the time is now to automate process the master data management and regulatory submission.
Therefore, we recommend watching the webcast from p36 and SAP to be the first to hear how to develop a company-wide and global strategy for centrally managing UDI product data using process automation to achieve and ensure global UDI compliance within your company.
We will discuss the challenges and opportunities of UDI compliance and how technology can help:
Manage the complexity of UDI compliance across many countries in one platform
Maintain efficient data government processes
Ensure global UDI compliance in the long-term
Click here to get early access to the webcast now!
SAP and p36 are aware of the multiple challenges and complexities life sciences organizations are facing with regard to UDI.
We hope you find this discussion insightful and that we have been able to show you that there are ways to ensure not only your global UDI compliance but also your competitiveness.