Location and Date: Orange County, CA – 4 November 2015, 11:00am-11:40am PST – Portford Solutions Group
Portford Solutions Nick & Bruce Bolton and Axcent Advanced Analytics Joe Buonomo to co-host an online event about how the rapidly changing FDA regulatory requirements affecting medical device tracking will be accommodated by Portford Solutions’ agile-based development strategy and implementation for their best-in-class SaaS solution.
The first in a series of Webinars to be held on November 4, 2015 to discuss the important regulatory requirement of coming into compliance for with the new FDA regulation for Unique Medical Device Identifier requirements. Portford Solutions will be sponsoring this first in a new Symposium series and will discuss how their current offering complies with the beginning of the FDA requirements for device tracking. Central to this offering is the creation of a Software as a Service (SaaS) platform, a cloud-based solution that is a best-in-class model for both its cost-effectiveness and ease of deployment to solve a wide range of medical device business challenges.
ApplicationXtender v8.0 Usability Enhancements
/in News, Software /by Bruce BoltonApplicationXtender v8.0 is now available and features a new, intuitive, HTML 5-based user interface (UI) that fully supports IE, Chrome, Safari, and Firefox.
So what’s so intuitive about it? See for yourself with these screen shots below and let us know if you want to see a demo.
AX 8.0 Interface
Left Navigation Panel
Features categories to quickly choose Applications and recently used queries
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Webinar: Tracking Medical Devices – How to Manage UDI Compliance Readiness
/in Medical Device Tracking, News /by Bruce BoltonLocation and Date: Orange County, CA – 4 November 2015, 11:00am-11:40am PST – Portford Solutions Group
Portford Solutions Nick & Bruce Bolton and Axcent Advanced Analytics Joe Buonomo to co-host an online event about how the rapidly changing FDA regulatory requirements affecting medical device tracking will be accommodated by Portford Solutions’ agile-based development strategy and implementation for their best-in-class SaaS solution.
The first in a series of Webinars to be held on November 4, 2015 to discuss the important regulatory requirement of coming into compliance for with the new FDA regulation for Unique Medical Device Identifier requirements. Portford Solutions will be sponsoring this first in a new Symposium series and will discuss how their current offering complies with the beginning of the FDA requirements for device tracking. Central to this offering is the creation of a Software as a Service (SaaS) platform, a cloud-based solution that is a best-in-class model for both its cost-effectiveness and ease of deployment to solve a wide range of medical device business challenges.
Medical Device Tracking: Rapidly Changing USA and Worldwide Regulatory Environment
/in DocuNECT, Medical Device Tracking, News /by Bruce BoltonThe September 2013 FDA Final Rule on UDIs for medical devices is now law! So what does this mean for Medical Device industry? It means that imminently, medical device manufacturers will have to upgrade their labeling and packaging systems along with their data management capabilities in order to stay compliant with incoming regulations and […]