Episode 4: ISO vs. cGMP vs. FDA Requirements

August 7, 2020

In Episode 4 of this 10-part series, Product Owner Manager Dave Latimer and Principal Product Management Director Terrance Holbrook discuss FDA requirements and how to comply with them. Key takeaways include: • Bridging the gap between quality and manufacturing. • Improving compliance processes. • Enhancing best practices to avoid common pain points. Watch other episodes here… https://www.mastercontrol.com/learning-center/manufacturing-webinar-series Subscribe for more informative content http://bit.ly/2RZAtKa Find out more about totally paperless production here. https://www.mastercontrol.com/library/white-papers/manufacturing-software-and-paperless-imperative/ Learn more about pharmaceutical compliance here. https://www.mastercontrol.com/learning-center/data-sheets/pharmaceutical-cgmp-for-21st-century MasterControl Inc. is a leading provider of cloud-based quality and compliance software for life sciences and other regulated industries. Our mission is the same as that of our customers – to bring life-changing products to more people sooner. The MasterControl Platform helps organizations digitize, automate and connect quality and compliance processes across the regulated product development life cycle. Over 1,000 companies worldwide rely on MasterControl solutions to achieve new levels of operational excellence across product development, clinical trials, regulatory affairs, quality management, supply chain, manufacturing and postmarket surveillance. For more information, visit https://www.mastercontrol.com/

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