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Article CommentaryCommentary

Risk-based Strategy to Determine Testing Requirement for the Removal of Residual Process Reagents as Process-related Impurities in Bioprocesses

Jinshu Qiu, Kim Li, Karen Miller and Anil Raghani
PDA Journal of Pharmaceutical Science and Technology May 2015, 69 (3) 334-345; DOI: https://doi.org/10.5731/pdajpst.2015.01056
Jinshu Qiu
1Product Development, Amgen Inc., Thousand Oaks, CA USA; and
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  • For correspondence: jqiu@amgen.com araghani@amgen.com
Kim Li
2Environment, Health, Safety and Sustainability, Amgen Inc., Thousand Oaks, CA USA
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Karen Miller
1Product Development, Amgen Inc., Thousand Oaks, CA USA; and
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Anil Raghani
1Product Development, Amgen Inc., Thousand Oaks, CA USA; and
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  • For correspondence: jqiu@amgen.com araghani@amgen.com
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PDA Journal of Pharmaceutical Science and Technology: 69 (3)
PDA Journal of Pharmaceutical Science and Technology
Vol. 69, Issue 3
May/June 2015
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Risk-based Strategy to Determine Testing Requirement for the Removal of Residual Process Reagents as Process-related Impurities in Bioprocesses
Jinshu Qiu, Kim Li, Karen Miller, Anil Raghani
PDA Journal of Pharmaceutical Science and Technology May 2015, 69 (3) 334-345; DOI: 10.5731/pdajpst.2015.01056

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Risk-based Strategy to Determine Testing Requirement for the Removal of Residual Process Reagents as Process-related Impurities in Bioprocesses
Jinshu Qiu, Kim Li, Karen Miller, Anil Raghani
PDA Journal of Pharmaceutical Science and Technology May 2015, 69 (3) 334-345; DOI: 10.5731/pdajpst.2015.01056
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  • Challenges and Solutions to Manufacturing of Low-Viscosity, Ultra-High Concentration IgG1 Drug Products: From Late Downstream Process to Final Fill Finish Processing
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Keywords

  • Clearance testing strategy
  • Process reagents
  • Process-related impurity
  • Safety margin
  • GRAS reagents
  • PSC reagents

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