Proceedings of the 2017 Viral Clearance Symposium Session 5: Facility Risk Mitigation

Junfen Ma; Thomas R. Kreil

doi:10.5731/pdajpst.2018.009175

Research ArticleProceedings of the 2017 Viral Clearance Symposium

Proceedings of the 2017 Viral Clearance Symposium Session 5: Facility Risk Mitigation

Junfen Ma and Thomas R. Kreil

PDA Journal of Pharmaceutical Science and Technology September 2018, 72 (5) 511-515; DOI: https://doi.org/10.5731/pdajpst.2018.009175

Junfen Ma

1Shire, Process Development and Technical Services, 300 Shire Way, Lexington, MA 02421, USA; and

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For correspondence: junfen.ma@shire.com

Thomas R. Kreil

2Shire, Global Pathogen Safety, Benatzkygasse 2-6, Vienna 1220, Austria

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1.↵
1. Knotzer S.,
2. Kindermann J.,
3. Modrof J.,
4. Kreil T. R.
Measuring the effectiveness of gaseous virus disinfectants. Biologicals. 2015, 43 (6), 519–523.
OpenUrl
2.↵
Viral safety evaluation of biotechnology products derived from cell lines of human or animal origin, Q5A (R1).
3.↵
Guidance for Industry, Q7 Good manufacturing practice guidance for active pharmaceutical ingredients.

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PDA Journal of Pharmaceutical Science and Technology

Vol. 72, Issue 5

September/October 2018

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Proceedings of the 2017 Viral Clearance Symposium Session 5: Facility Risk Mitigation

Junfen Ma, Thomas R. Kreil

PDA Journal of Pharmaceutical Science and Technology Sep 2018, 72 (5) 511-515; DOI: 10.5731/pdajpst.2018.009175

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Proceedings of the 2017 Viral Clearance Symposium Session 5: Facility Risk Mitigation

Junfen Ma, Thomas R. Kreil

PDA Journal of Pharmaceutical Science and Technology Sep 2018, 72 (5) 511-515; DOI: 10.5731/pdajpst.2018.009175

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