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About ComplianceQuest
ComplianceQuest is the #1 AI-powered Quality, Risk, and Compliance (QRC) platform that connects Product, Quality, Manufacturing, People, Suppliers and Customers in a single system.
Built on Salesforce, the platform delivers end-to-end visibility, AI-driven intelligence, and enterprise-scale execution, enabling organizations to manage risk, ensure regulatory compliance, and turn quality into a driver of growth.
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It was a breezy morning in late November 2019 in Miramar, FL. The Director of Regulatory Affairs and Quality Systems of an exciting software-based medical device company received a phone call from the executive leadership and board members. They got straight to the point.
“We need a robust, automated software solution to meet our quality, safety and regulatory requirements.” The board members then put down an aggressive timeline: “This needs to be ready for use by April 2020.”
The Director of Quality had no time. He immediately got to work and jotted down on his notepad a set of requirements he would use to evaluate several Quality, Health, Safety and Environment Solution providers. One criterion was non-negotiable – a solution that would work out of the box or with minimum customization. His timelines demanded that.
With that as the first requirement, he invited several EQMS and QHSE solution providers for a pitch. One of the companies he invited was ComplianceQuest. Eventually, the software-based medical device company decided to go with our solution for the following reasons:
It has been over a year and a half since we deployed ComplianceQuest at various locations across the country. While the initial goal was to launch on time and move from a paper-based system to automation, today the company uses our QHSE solution to deliver a competitive advantage and drive-up customer satisfaction. The executive leadership team at the customer organization is also extremely satisfied with ComplianceQuest’s analytics capabilities and the robustness of our Complaints Solution.
“The out-of-the-box features help us determine if an event is reportable. If it is, a task is created, and you are prompted to fill in details that the FDA requires. Once that’s complete, it will create the XML file to load into the FDA’s reporting system. This was wild to me.”
Director of Regulatory Affairs and Quality Systems, Arc One
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