How Bio-Rad harmonized global clinical workflows with unified eTMF

Managing clinical trials across regions poses challenges for medical technology companies, including documentation discrepancies, inconsistent processes, and compliance risks that threaten study integrity.

Bio-Rad Laboratories addressed these issues by adopting a unified electronic Trial Master File system, showcasing how standardized global processes reduce compliance risks. This case study highlights their approach to harmonizing operations while integrating quality and clinical workflows. Key insights include:

· Reducing documentation inconsistencies
· Integrating quality and clinical workflows
· Standardizing global processes

Learn how Bio-Rad transformed clinical operations.