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  • Quality Assurance and Regulatory Aspects of HPLC in Quality

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Thursday - Jul 25, 2013 07:00 AM
  • End Time:
  • Thursday - Jul 25, 2013 08:30 AM
  • Location:
  • Online
  • This webinar will cover the regulatory requirements for cGLP cGMP HPLC analysis, provide practical tips for compliance, common pitfalls in analyses and show how to manage adverse audit findings.

    Why Should You Attend:

    This presentation will help you meet FDA, ICH and other regulatory requirements for the Quality Assurance and Quality Control for Testing of Pharmaceutical API and or Nutritional Supplement ingredients to validate potency claims. It will help you better understand how to meet and maintain these requirements in a cost effective way to avoid adverse audit findings.

    Learning Objectives:

    - To understand the regulatory requirements for cGLP cGMP HPLC analysis and the reasons for them
    - To learn of cost effective ways to implement and maintain the required compliances
    - To understand why analyses performed with systems not properly Qualified and or using methods that are not properly validated will result in questionable results, adverse audit findings, and jeopardize the validity of QC and Stability Testing results necessary for correct product testing and release.
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