Making the Switch: The Evaluation, Implementation and Validation of Bringing Rapid Mycoplasma Testing In-House to Expedite Lot Release of Recombinant Protein Product

Previously Aired on May 19th, 2020

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Overview

Octapharma AB in Stockholm, Sweden, is the site for the NUWIQ® production, a recombinant human FVIII produced in human cells. Regulatory guidelines state that recombinant bulk harvest must be tested for mycoplasma prior to further processing. This presentation will give an overview of Octapharma’s journey on replacing an out-sourced mycoplasma test with an in-house mycoplasma qPCR assay. Octapharma received regulatory approval for the assay in October 2019 and plan to run in-house mycoplasma testing for lot release, hence saving lead time for their recombinant production.

The presentation will share Octapharma’s evaluation of the PCR method, as an alternative to the traditional growth-based mycoplasma testing and the process of laboratory set-up and instrument qualifications and software requirements. Finally, a summary of the method development, validation, ensuring assay sensitivity met regulatory requirements, and regulatory submission process will be presented.

Presenters

Presenter
Kent Persson, PhD
(Speaker)
Project Manager,
Octapharma AB
View Biography
Presenter
Mike Auerbach
(Moderator)
Editor-in-Chief,
American Pharmaceutical Review