04.08.15
St. Louis, Mo.-based Biomedical Systems, which provides centralized diagnostic systems and clinical trial support to medtech companies, has begun a partnership with the Electronic Patient-Reported Outcome (ePRO) Consortium, a program run by the Critical Path Institute (C-Path).
Biomedical Systems will collaborate with the group’s 10 other members to advance the quality, practicality and acceptance of electronic data capture methods used in clinical trials for PRO endpoint assessment.
“Clinical outcome assessments are becoming more important in clinical trials to determine whether a drug has demonstrated a treatment benefit,” said Timothy Barrett, chief operating officer at Biomedical Systems. “By joining the ePRO Consortium, Biomedical Systems will contribute in a non-competitive and neutral environment to improve the quality of data collection methods for clinical outcomes assessments.”
Biomedical Systems’ second generation ePRO platform supports home, site and Web-based systems to collect timely, high-quality data for clinical trials around the world.
C-Path is a nonprofit, public-private partnership with the U.S. Food and Drug Administration (FDA). Its goal is to bring scientists from the FDA, industry and academia together to improve the drug development and regulatory process for medical products. The institute was founded in 2005.
Created in 2011, C-Path established the ePRO Consortium in cooperation with firms that provide technologies and services for capturing patient-reported outcome endpoints.
“We look forward to the new relationships and opportunities our membership in the ePRO Consortium will create for our team and our industry,” said Barrett.
Biomedical Systems will collaborate with the group’s 10 other members to advance the quality, practicality and acceptance of electronic data capture methods used in clinical trials for PRO endpoint assessment.
“Clinical outcome assessments are becoming more important in clinical trials to determine whether a drug has demonstrated a treatment benefit,” said Timothy Barrett, chief operating officer at Biomedical Systems. “By joining the ePRO Consortium, Biomedical Systems will contribute in a non-competitive and neutral environment to improve the quality of data collection methods for clinical outcomes assessments.”
Biomedical Systems’ second generation ePRO platform supports home, site and Web-based systems to collect timely, high-quality data for clinical trials around the world.
C-Path is a nonprofit, public-private partnership with the U.S. Food and Drug Administration (FDA). Its goal is to bring scientists from the FDA, industry and academia together to improve the drug development and regulatory process for medical products. The institute was founded in 2005.
Created in 2011, C-Path established the ePRO Consortium in cooperation with firms that provide technologies and services for capturing patient-reported outcome endpoints.
“We look forward to the new relationships and opportunities our membership in the ePRO Consortium will create for our team and our industry,” said Barrett.