Did you know you can use our actionable intelligence to identify and control risk with your critical GLP, GCP, GDP, and GMP vendors as part of your vendor monitoring strategy?
With more than 300,000 unique Site Profiles across GXPs, you will never be in the dark about your vendors’ regulatory history and their most up-to-date inspection information.
Below we offer a look into a case study that shows how a leading distributor and medical device manufacturer uses our data to help prequalify vendors and continuously monitor them over the course of their partnership to stay in regulatory compliance.
One of the largest U.S.-based distributors and medical device manufacturers with over 10,000 suppliers needed to improve its supplier risk assessment and monitoring program in order to ensure FDA compliance and improve patient safety.
Visiting supplier sites was not only labor and time-intensive but also impossible due to pandemic restrictions.
For supplier qualification, the company turned to Redica’s Enforcement Analytics to leverage our Site and Organization profiles to understand and analyze the full regulatory history of its suppliers, ensuring that it adds quality into its purchasing decisions.
For ongoing monitoring, the Redica Customer Success team helped to build a monitoring portfolio of over 5,000 suppliers. Our system automatically sends notifications for any inspection or enforcement event.
The company experienced an immediate benefit, with a time-to-value of less than one week as an onsite audit was determined not to be necessary due to Redica’s data.
The company now has demonstrable compliance with supplier evaluation and monitoring needs.
Want to see how Redica can help with your vendor monitoring? Contact us for a personal tour of Enforcement Analytics and see how you can monitor your suppliers without getting on a plane.
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