Portford Solutions Introduces: DocuNECT for Device Tracking
Medical Device manufacturers are required by the FDA to track certain types of devices from manufacture through the distribution chain. The FDA released 21 CFR Part 821, which governs the requirements around the tracking process.
Flexible Software Solutions
• On-Site: Software implemented behind your firewall
• Hosted: A SaaS model where you can pay monthly
Outsource Your Process
Portford also offers a complete managed service that combines the SaaS model with our call-center of trained device tracking specialists that will manage the entire process. Our services begin with fully documented policies and procedures that aid with FDA compliance.
Each client is allowed to customize the workflow to meet the profile of your device or specific needs. The operations team then follows these policies and procedures and conduct regular audits to verify compliance. We have a wide variety of reports and reporting methods which employ industry standards and tools.
DocuNECT for Device Tracking – Overview and Demonstration
Join us to learn about Portford’s DocuNECT solution for 21 CFR Part 821. Space is limited!
WHEN: 9/7/11 at 10:00am PST.
WHERE: Online Webinar via WebEx.