Validation Master Plan For Filtration Systems Used In Aseptic Processing
Source: MilliporeSigma
Regulatory guidance provides a framework for aseptic processing that ensures patient safety.
Developing a sterile filtration process starts with selection of the appropriate filtration system and qualification of filter performance. It continues with good engineering and validation practices and the establishment of standard operating procedures (SOPs), training of operators, and ongoing adherence to documented procedures.
Explore a general master plan that summarizes best practices for validating performance of critical filtration systems used in aseptic processing.
access the White Paper!
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 Biosimilar Development? Subscribe today.
Subscribe to Biosimilar Development
X
Subscribe to Biosimilar Development
MilliporeSigma
This website uses cookies to ensure you get the best experience on our website. Learn more