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marcus evans
Published: Wednesday, August 17, 2016 - 13:58 (marcus evans: London) -- 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 the conference, “Quality Risk Management & Process Validation in the Product Life Cycle,” which will be held Sept. 28–30, 2016, in Berlin.
This conference will help attendees to implement a quality risk management approach into their existing quality systems. It will also provide a better understanding of how to assess and evaluate risks in their companies and with third-party partners. By attending this conference, attendees will be able to be part of more than 14 hours of focused, end-user-driven case studies, 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 are: Read the interview with conference guest speaker Michael Schousboe, principal specialist, quality risk management at Novo Nordisk. For more information about this event, contact Yiota Andreou at yiotaa@marcusevanscy.com and visit the event website here. Quality Digest does not charge readers for its content. We believe that industry news is important for you to do your job, and Quality Digest supports businesses of all types. However, someone has to pay for this content. And that’s where advertising comes in. Most people consider ads a nuisance, but they do serve a useful function besides allowing media companies to stay afloat. They keep you aware of new products and services relevant to your industry. All ads in Quality Digest apply directly to products and services that most of our readers need. You won’t see automobile or health supplement ads. So please consider turning off your ad blocker for our site. Thanks, marcus evans is one of the world’s leading providers and promoters of global summits, strategic conferences, professional training, in-company training, business-to-business congresses, sports hospitality, and on-line information.Implement an Efficient Pharmaceutical Quality Risk Management System
Sept. 28–30, 2016, in Berlin
• Effectively integrate ICH Q8, Q9, Q10, and Q11 guidelines into the quality system
• Discuss regulatory expectation on process validation
• Define an efficient quality risk management system and tools across the global quality system
• Design efficient processes to ensure quality control
• Correctly handle third-party partners within quality risk management processes
• Apply efficient continuous process verification to monitor the system
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