Case Study

Tekton Research Experiences A 'No Findings' FDA Inspection

Source: Complion
For Regulatory Retention Compliance In Life Science Industries And Clinical Trial Research

As COVID-19 increased its impact on research collaboration and monitoring in 2020, Tekton Research’s desire to move to full remote monitoring intensified. The research site soon realized there was a need for a remote source document monitoring solution --– one that would enable the upload, management and sharing of source documents with monitors and sponsors without redacting sensitive patient information.

That’s when Tekton made the call to Complion, Inc., the leading provider of eRegulatory (eISF) solutions for high-performing research sites, sponsors and CROs. To date, Tekton has used Complion to create more than 20 patient source document binders built specifically for remote monitoring.

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