Episode 5: FDA Current Guidance and Exemptions

August 7, 2020

In Episode 5 of this 10-part series, Product Owner Manager Dave Latimer and Principal Product Management Director Terrance Holbrook talk specifically about how digitizing helps with the complexity of compliance. Key takeaways include: • How to be audit ready. • Requirements of 21 CFR 210-211. • How digitizing streamlines processes. Watch other episodes here… https://www.mastercontrol.com/learning-center/manufacturing-webinar-series Subscribe for more informative content http://bit.ly/2RZAtKa Learn how regulators are digitizing. https://www.mastercontrol.com/library/white-papers/fda-cloud-trends-2020/ Read about the biggest pharmaceutical trends of 2020. https://www.mastercontrol.com/library/white-papers/pharma-trends-2020/ 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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Episode 4: ISO vs. cGMP vs. FDA Requirements
Episode 4: ISO vs. cGMP vs. FDA Requirements

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Episode 3: Achieving and Maintaining an Audit-Ready State
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