Sharing of the Fernald Community Cohort Data and Biospecimens
The availability of the data and biospecimens of the Fernald Community Cohort for future research studies has been communicated by presentations at various scientific meetings and through listing on ClinicalTrials.gov.
Research investigators interested in using the FCC database and samples for health-related research may apply for Access to Data and/or Biological Specimens. If approved by the Research Director, with the advice of the Fernald Community Cohort Advisory Committee, data files from the FCC database or archived samples (frozen whole blood, serum, plasma and urine) may be distributed to qualified researchers.
Any individual or group desiring access to the FCC database or archived samples for purpose of conducting a research study must first submit an application to the FCC Research Director, Dr. Susan M. Pinney, who, in turn, will first obtain input from the Fernald Community Cohort Advisory Committee. Pdf files of the FMMP Access to Data and Specimens Policy are below.
- Access to Data Policy (PDF)
- Access to Data Application for Primary Investigator/PI (DOC, Word File)
- Access to Data Application for Co-Investigator/CoI (DOC, Word File)
- FCC Database & Biospecimen Costs (PDF)
- Read More - Strengths of the Fernald Community Cohort as a Research Resource (PDF)
ClinicalTrials.gov PRS
Protocol Registration and Results System
Sponsor | University of Cincinnati |
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Collaborators | National Institute of Environmental Health Sciences(NIEHS) |
Information provided by (Resposible Party) | Susan Pinney, University of Cincinnati |
ClinicalTrials.gov Identifier |
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Phone: 513-558-5701