Software Validation Keeps GxP Systems Current And Speeds Up Time-To-Market
Source: IDBS UK HQ
By Fran Carmody, Services Enablement Manager, IDBS
Product software validation is a process that ensures a software product meets a user’s demands and expectations. As of 2002 the FDA requires that pharmaceutical companies demonstrate and document that their software accurately and consistently produces quality results. The challenge is that validating new software, such as a laboratory information management system (LIMS), can take up to a year to complete.
Explore what a risk-based approach to software validation is and a cloud-based platform that can help you to complete your validations. faster.
access the Article!
Log In
Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue.
X
Enter your credentials below to log in. Not yet a member of Bioprocess Online? Subscribe today.
Subscribe to Bioprocess Online
X
Subscribe to Bioprocess Online
IDBS UK HQ
This website uses cookies to ensure you get the best experience on our website. Learn more