RegulatoryBinder saves hospitals time and money spent on research documentation.
The Clinical Trials Transformation Initiative and Institute of Medicine, however, have recently said that clinical research is a "paper-based, slow, & costly" "burden" on hospitals already under increasing cost-constraints.
Limited revenue-generators at hospitals, spend copious amount of time managing printed pages of regulatory documentation in three-ring regulatory binders! This represents a $50B documentation opportunity cost.
RegulatoryBinder has developed a novel SaaS solution that enables staff to reduce the time spent on research documentation by 33%, resulting $15B in potential annual savings. Only RegulatoryBinder is designed for hospital regulatory binders and bundles compliance services to ensure that software is compliant with FDA eRecord regulations from the very first login. Existing software can take $3-5M and over 1 year to customize, validate, and implement.