(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.

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