HomeWebinarsValidation of Tangential Flow Filtration in Biotech Processes

Validation of Tangential Flow Filtration in Biotech Processes


Tangential flow filtration (TFF) is a unit operation that is used in monoclonal antibodies, recombinant proteins, and vaccine processing for ultrafiltration-diafiltration and/or clarification. In order to ensure the safety and efficacy of the drug, validation of the unit operations used in manufacturing is mandatory and a part of the regulatory requirement. The objective of validation of a unit operation is to demonstrate with a high degree of confidence that the process performs consistently. The present seminar will focus on the validation of the unit operation of TFF and will provide an overview of the regulatory landscape, the validation master plan, approaches to membrane re-use, cleaning validation, and best practices.

In this webinar, you will learn about:

  • Validating TFF
  • Validating a master plan
  • Membrane reuse and cleaning
  • TFF scale-down models


Subhasis Banerjee, Ph.D.

Subhasis Banerjee, Ph.D.


Principal Bioprocessing Application Expert

Subhasis supports the technical consultation for downstream processing for the APAC region. He has a Ph.D. in biochemistry with post-doctoral experience from The Ohio State University, Columbus, USA. He has contributed to several publications in international peer-reviewed journals and conducted presentations in numerous national and international Conferences.

Webinar Information

Pharma and biopharma manufacturing

  • Liquid Formulation Strategies
  • Duration:1h

  • Language:English

  • Session 1:presented July 13, 2021

    Watch Now

Sign In To Continue

To continue reading please sign in or create an account.

Don't Have An Account?