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Avoid FDA Recalls: A Connected QMS & EBR Roadmap

Join us for a webinar with MasterControl on mitigating risks, protecting patient safety, and maintaining regulatory compliance.

Avoid FDA Recalls: A Connected QMS & EBR Roadmap
Published: | 2 min read

JOIN THE EXPERTS: NOVEMBER 7TH 2024 | 09:00 EST | 14:00 GMT | 15:00 CET 


FDA-initiated recalls have increased 115% since 2018, and consumers have taken note. Recent surveys show that nearly half of survey respondents do not have confidence in the manufacturing process and quality of their medications. And over half wouldn’t purchase a product that was previously recalled. This negative consumer sentiment presents an uphill battle for life sciences manufacturers who don’t have the right solutions in place. Join us to learn more about the common issues that can lead to a recall and how MasterControl’s connected quality management system (QMS) and electronic batch record (EBR) solution can help you prevent them and instil consumer confidence. 


MasterControl Inc. is a leading provider of cloud-based quality and manufacturing software for life sciences and other regulated industries. For three decades, our mission has been the same as that of our customers – to bring life-changing products to more people sooner. MasterControl helps organizations digitize, automate, and connect quality and manufacturing processes. Innovative MasterControl tools have a proven track record of improving product quality, reducing cost, and accelerating time to market. Over 1,100 companies worldwide use MasterControl solutions to streamline operations, maintain compliance, easily analyze and interpret large amounts of data, and visualize business insights in real time. For more information, visit www.mastercontrol.com. 



Speakers 


Matt Lowe | Chief Strategy Officer | MasterControl


Matt Lowe has served MasterControl for nearly two decades across several different executive leadership roles including product, engineering, sales, and marketing, and now will continue his tenure as Chief Strategy Officer. He also serves on the MasterControl Board of Directors. 


Lowe is a  medical device expert with experience in product development and product management at Ortho Development Corp. and Bard Access Systems, a subsidiary of BD. Lowe has successfully launched more than a dozen medical devices. He has five patents issued and one pending. His regulatory experience includes writing a 510(k) that was cleared by the FDA and managing a multi-site, multi-year post-market clinical study for orthopaedic devices. 



Dallas Volk  | Solutions Consultant  | MasterControl


Dallas Volk has two decades of experience in life science manufacturing and quality systems, helping quality organizations to identify, implement and validate technology solutions that have enabled them to achieve their compliance initiatives. As a Solutions Consultant at MasterControl, he uses his extensive quality and manufacturing knowledge to give prospects and customers alike accurate demonstrations of MasterControl solutions and how they solve regulatory and compliance challenges while making users’ system experiences hassle-free. 


Prior to MasterControl, Dallas held many different quality roles in the pharmaceutical and aerospace industries, including being a Quality Engineer for a medical device manufacturer and Quality Inspection team member for the Air Force National Guard.  

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Med-Tech Insights Staff

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