Next Generation Sequencing (NGS) technology has taken center stage on the world platform as a suitable alternative methodology to traditional broad virus safety screening in biologically derived products as both the industry and regulators progress initiatives to replace, reduce, and refine (3Rs) animal testing. Global industry and interest groups have been working for over a decade to demonstrate the suitability of the technology to serve as a primary virus screening method.
As a result, NGS-based methods have been used for virus detection for many years to ensure the safety of both clinical and commercial products. Recent updates to the ICH Q5A virus safety guidance encourage the use of NGS as a replacement for in vivo and in vitro adventitious testing methods.
The revised guidelines provide the expectations of a well-validated method that can be used for the detection of known and unknown viruses. In this presentation, we will discuss the drivers behind the use of the technology, our approach to the validation of an NGS-based adventitious agent method, and the robust bioinformatic analysis that makes it all possible.
In this webinar, you will learn:
- The regulatory drivers and worldwide initiatives behind the movement to NGS-based virus testing methods
- How the methodology and bioinformatics is validated for its intended purpose and applied in the highly regulated GMP environment
- Hear about real-life case studies showcasing the use of the technology to ensure virus safety in biological products
Pharma and biopharma manufacturing
- Pharma and biopharma manufacturing
기간:1h
언어:English
세션 1:발표 완료 December 12, 2023
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