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      GMP University - Internal Audits and FDA Inspections in San Diego

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      August 19, 2019

      Monday  12:00 PM

      San Diego, California, United States
      San Diego, California

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      GMP University - Internal Audits and FDA Inspections

      Make Key Decisions Based on an Effectively Managing Risks in Your Quality System Risk management is a key component to your Quality Management System, a regulatory requirement and one that has critical impact on your organization. KENX is excited to announce a conference the can dramatically affect your strategy surrounding your risk management program. KENX’s Quality Risk Management conference provides the knowledge and tools to develop, implement and maintain best-in-class procedures that impresses FDA investigators, benefits your organization and expands your professional development. This program guides you through the process of evaluating, managing and mitigating risks to your quality system. Top 10 Reasons to Attend: Regulatory intelligence – Stay up to speed on regulatory thinking Know ICH guidelines and why you should care Discover the most under-utilized QRM tool in industry Minimize subjectivity is risk assessments Present your QRM program to an inspector Learn how to structure QRM training See Bayer’s journey toward a robust QRM program Go beyond FMEA – QRM tools you should be using (but aren’t) Create custom risk tools/risk-based approaches Go well beyond ICH Q9 and the basics Personnel in the Following Environments Should Attend: QA/QC Risk management Regulatory affairs Compliance and auditing Internal auditing Quality engineers Manufacturing Laboratory This event is also appropriate to business development and sales managers that offer innovative solutions for change control, risk management, statistics and validation.

      Categories: University & Alumni

      Event details may change at any time, always check with the event organizer when planning to attend this event or purchase tickets.