Overview

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Portford provides a range of document management solutions for any size of Life Science organization that manage the lifecycle of regulated documents. The solution is modular and ideal for small organizations to get started with document management and to scale to a full compliance enterprise document management solution.

Portford's consulting group provides a complete range of Computer System Validation (CSV) services for the following  areas:

 
  • GxP Document Management Systems
  • Medical Device Tracking
  • Compliance and Quality Solutions
  • Regulatory Submissions Support
  • Computer System Validation
 
What Can We Do? Quick Links...
   
  • Provide document management systems to manage GxP documents with 21 CFR Part 11 Compliance Electronic Signatures
  • Outsourced services and software for a Secure Due Diligence Portal
  • Outsourced services and software for Medical Device Tracking (CFR 21 Part 820 compliant)
  • Federal DOD 5015.2 records management and retention capabilities
  • Provide software to manage all aspects of the Quality and Risk management process
  • eDiscovery solutions for automated discovery
The right choice for life science companies
We’ve been earning customer acclaim for our document management and scanning services, and our technical expertise and breadth of partnerships allow us to configure the right solution for you! 
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