Make Key Decisions Based on an Effectively Managing Risks in Your
Quality SystemRisk 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._
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22/08/2019 Last update