The challenge of implementing MES technology with increased regulation

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In a recent article published by Contract Pharma our manufacturing expert
Christian Fortunel discusses how drug manufacturers face a unique set of challenges
when managing their operations, which continue to evolve as regulations tighten, new trends develop and IT spending comes under greater scrutiny.

In any contract manufacturing environment, time is money, and therefore opportunities to improve efficiencies and increase productivity must be explored. In addition, the pharmaceutical industry faces increasingly stringent regulations, making compliance a priority when implementing new technology. By creating a centralized point of information in line with GMP standards and allowing real-time production visibility and instant reporting, MES can help to simplify the compliance process.

Those companies that embrace new technologies can be both compliant and competitive in an extremely fast-moving and continually evolving environment.

Read the full article to discover the benefits of adopting a technology-based approach to manage manufacturing operations in real-time.