Clinical Testing Laboratory

Our Clinical Trials testing is conducted in compliance with Good Clinical Laboratory Practice (GLP) and is crafted to meet your specific needs. Throughout the study our Principal Investigator will keep you updated on the progress of testing and notify you in a timely manner as to when the study should be finished.

All testing is conducted on healthy human subjects and takes place in one of our two clinical specific laboratories. Prior to recruitment of subjects, clinical studies require the approval of the Gallatin Institutional Review Board (GIRB), a group of individuals not employed by Nelson Labs Bozeman , but with whom Nelson Labs Bozeman contracts to review study protocols. The GIRB operates with the specific objective of ensuring subject safety. In addition, Nelson Labs Bozeman works with two consulting physicians who ensure that all human subjects recruited are fit to test with us.

At the end of each study, the Principal Investigator will develop a final report package that includes the test protocol, study data, applicable statistical analysis and a summary report. All paperwork associated with the study will be available for you to view. Each final report package will also be reviewed by our Quality Assurance department and Senior Scientific staff.

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