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  • Forced Degradation Studies/ Biologics Stability Programs for

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Thursday - Oct 03, 2013 10:00 AM
  • End Time:
  • Thursday - Oct 03, 2013 11:30 AM
  • Location:
  • Online
  • This 90-minute training will provide you with an overview of a forced degradation study on a protein therapeutic and help you interpret and leverage the results to design stability studies required for registration of the BLA.

    Why Should You Attend:
    A comprehensive forced degradation study is essential for design of an Analytical Program which when implemented right from the initial stages of a project will result in Right-first -time CMC data package and therefore lead to cost savings in terms of Analytical Lab and Regulatory Department resource requirements. The forced degradation results must be incorporated in the design of the compliant stability program which is essential for the success of a well characterized protein product.

    This 90 Min session is designed to provide the attendee with an overview of a forced degradation study on a protein therapeutic and to interpret and leverage the results to design the Stability Studies required for registration of the BLA. The speaker will address the stress conditions typically used to study the tendency of the protein to undergo degradation along with the analytical methods required for the study. Forced degradation study data must be utilized during the design of the stability program. We will discuss how you can leverage the forced degradation results to design stability studies for the drug Substance and drug Product. The regulatory requirements for such studies will be addressed.

    Areas Covered in the Seminar:
    What is the purpose of a Forced degradation study?
    What are the conditions to be used during well characterized protein forced degradation study?
    How to test for the degradants?
    Design of a compliance wcp stability study based on the forced degradation results.
    Conduct of a biologics stability study.
    Common mistakes during forced degradation studies.

    Who Will Benefit:
    Stability department personnel
    R&D Laboratory personnel
    R&D Laboratory Supervisors and Management
    QC Laboratory personnel and management
    Protein Formulation Group personnel and Management
    Regulatory Affairs personnel
    Regulatory Affairs Management
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