Regulatory Guidance For Bioprocessing Software
Source: MilliporeSigma
Use of software in a biopharmaceutical GxP environment provides many benefits to users and the organization, but also comes with stringent regulatory requirements.
This talk highlights some of those regulatory requirements and describes how software is invaluable for creating an audit trail, reporting, and automating regulatory-related tasks.
access the Webinar!
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 Advancing RNA? Subscribe today.
Subscribe to Advancing RNA
X
Subscribe to Advancing RNA
MilliporeSigma
This website uses cookies to ensure you get the best experience on our website. Learn more