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    How to survive and thrive in FDA and EU inspections for GxP - Ask the expert

    Prepare for your next GxP inspection with confidence!

    Agenda

     

    14:47
    General Audit and Inspection Processes


    01:04:10
    Auditing Techniques and Answering Questions Effectively


    01:06:25
    Top FDA Drug Observations

    Watch an exclusive Ask Me Anything (AMA) session with Andrés Gola, Senior Consultant at PBSV, who brings 15 years of experience in FDA-regulated environments, specializing in quality systems, GMP, and FDA inspections. He answered the most pressing live and pre-submitted questions from the life sciences community, covering everything from pre-inspection preparations to post-audit compliance and the future of regulatory audits.

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      EMEA Office
      Louizalaan 489
      1050 Brussels
      Belgium

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      Scilife Inc.
      228 E 45th St. RM 9E
      New York, NY 10017

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