(marcus evans: London) -- The focus of pharmaceutical quality systems have shifted in recent years from a traditional model to a more global, dynamic, and risk-based approach, enhanced especially by regulatory authorities and economic environment. marcus evans is organizing “Quality Excellence: From Quality Risk Management to Continuous Process Verification” a unique conference to be held June 20–22, 2016, in Berlin. This conference will help attendees learn how to implement a quality risk management approach into their existing systems. It will also provide a better understanding on how to assess and evaluate risks in their companies and with third parties.
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By attending this conference, attendees will receive more than 14 hours of focused end-user-driven case studies and interactive panel discussions and workshops. In addition, delegates will have the opportunity to network with senior-level executives and learn about the latest developments and trends in pharmaceutical quality systems.
The key topic areas include:
• Regulatory expectation for quality compliance approaches
• Efficient quality risks management systems and tools across the global quality system
• Efficient processes to ensure quality control
• Third-party quality risk management processes
• Efficient continuous process verification and monitoring systems
Quality Digest Daily readers are eligible for a discount of 200 euros. For more information about this event, please contact Yiota Andreou at yiotaa@marcusevanscy.com or visit the event website and register using code LS152-QD to claim your discount.
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