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Research ArticleConference Report

Meeting Report: 2013 PDA Virus & TSE Safety Forum

Hannelore Willkommen, Johannes Blümel, Kurt Brorson, Dayue Chen, Qi Chen, Albrecht Gröner, Brian R. Hubbard, Thomas R. Kreil, Michel Ruffing, Sol Ruiz, Dorothy Scott and Glenda Silvester
PDA Journal of Pharmaceutical Science and Technology May 2014, 68 (3) 193-214; DOI: https://doi.org/10.5731/pdajpst.2014.00980
Hannelore Willkommen
aRegulatory Affairs & Biological Safety Consulting, Erzhausen, Germany;
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  • For correspondence: hannelore.willkommen@gmx.de
Johannes Blümel
bPaul-Ehrlich Institut, Langen, Germany;
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Kurt Brorson
cCDER/FDA, Silver Spring, MD, USA;
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Dayue Chen
dEli Lilly and Company, Indianapolis, IN, USA;
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Qi Chen
eGenentech Inc., South San Francisco, CA, USA;
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Albrecht Gröner
fCSL Behring GmbH, Marburg, Germany;
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Brian R. Hubbard
gAmgen Inc., Thousand Oaks, CA, USA;
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Thomas R. Kreil
hBaxter BioScience, Vienna, Austria;
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Michel Ruffing
iBoehringer Ingelheim Pharma GmbH&KG, Bieberach an der Riss, Germany;
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Sol Ruiz
jSpanish Medicines Agency (AEMPS), Madrid, Spain;
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Dorothy Scott
kCBER/FDA, Silver Spring, MD, USA; and
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Glenda Silvester
lEuropean Medicines Agency, London, UK
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Abstract

The report provides a summary of the presentations and discussions at the Virus & TSE Safety Forum 2013 organized by the Parenteral Drug Association (PDA) and held in Berlin, Germany, from June 4 to 6, 2013. The conference was accompanied by a workshop, “Virus Spike Preparations and Virus Removal by Filtration: New Trends and Developments”. The presentations and the discussion at the workshop are summarized in a separate report that will be published in this issue of the journal as well.

As with previous conferences of this series, the PDA Virus & TSE Safety Forum 2013 provided again an excellent opportunity to exchange information and opinions between the industry, research organizations, and regulatory bodies. Updates on regulatory considerations related to virus and transmissible spongiform encephalopathy (TSE) safety of biopharmaceuticals were provided by agencies of the European Union (EU), the United States (US), and Singapore. The epidemiology and detection methods of new emerging pathogens like hepatitis E virus and parvovirus (PARV 4) were exemplified, and the risk of contamination of animal-derived raw materials like trypsin was considered in particular. The benefit of using new sequence-based virus detection methods was discussed. Events of bioreactor contaminations in the past drew the attention to root cause investigations and preventive actions, which were illustrated by several examples. Virus clearance data of specific unit operations were provided; the discussion focused on the mechanism of virus clearance and on the strategic concept of viral clearance integration.

As in previous years, the virus safety section was followed by a TSE section that covered recent scientific findings that may influence the risk assessment of blood and cell substrates. These included the realization that interspecies transmission of TSE by blood components in sheep is greater than predicted by assays in transgenic mice. Also, the pathogenesis and possibility of productive TSE infection of cell substrates were considered, and cell-based assays that may be suitable for use in TSE clearance studies were discussed.

The current report provides an overview about the outcomes of the 2013 PDA Virus & TSE Safety Forum, a unique event in this field.

  • Virus
  • TSE
  • Safety
  • Biotechnology
  • Plasma derivatives
  • Regulatory affairs
  • Virus clearance
  • © PDA, Inc. 2014
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PDA Journal of Pharmaceutical Science and Technology: 68 (3)
PDA Journal of Pharmaceutical Science and Technology
Vol. 68, Issue 3
May/June 2014
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Meeting Report: 2013 PDA Virus & TSE Safety Forum
Hannelore Willkommen, Johannes Blümel, Kurt Brorson, Dayue Chen, Qi Chen, Albrecht Gröner, Brian R. Hubbard, Thomas R. Kreil, Michel Ruffing, Sol Ruiz, Dorothy Scott, Glenda Silvester
PDA Journal of Pharmaceutical Science and Technology May 2014, 68 (3) 193-214; DOI: 10.5731/pdajpst.2014.00980

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Meeting Report: 2013 PDA Virus & TSE Safety Forum
Hannelore Willkommen, Johannes Blümel, Kurt Brorson, Dayue Chen, Qi Chen, Albrecht Gröner, Brian R. Hubbard, Thomas R. Kreil, Michel Ruffing, Sol Ruiz, Dorothy Scott, Glenda Silvester
PDA Journal of Pharmaceutical Science and Technology May 2014, 68 (3) 193-214; DOI: 10.5731/pdajpst.2014.00980
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More in this TOC Section

  • Summary of the EMA Joint Regulators/Industry QbD workshop (London, UK; 28–29 January 2014)
  • Meeting Report: 2015 PDA Virus & TSE Safety Forum
  • PDA Single-Use Systems Cross-Organizational Workshop—Meeting Summary, May 14, 2014—PDA Global Headquarters, Bethesda, MD
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Keywords

  • Virus
  • TSE
  • Safety
  • Biotechnology
  • Plasma derivatives
  • Regulatory affairs
  • Virus Clearance

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