Tuesday, 1 December 2015

Inspection Readiness: Leveraging Inspection Focus Areas and Increasing the Transparency of Investigator Oversight

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An auditor's goal is to confirm the trial runs 
in a way that ensures the safety of the subjects, 
protects their rights and generates reliable data.

by Jessica Masarek

Quality Assurance Consultant | Independent Auditor

Director, Muse Clinical 



Audits and inspections seem to be wrapped in a shroud of mystery, making folks stressed and unsure of exactly what is going to happen.  What if I say the wrong thing?  What if I don’t know the answer?  What if I can’t provide what they are asking for?  Realistically, all of these things will probably happen!  That said, as long as you are honest, all will be well. Mistakes happen and no auditor or inspector is expecting perfection.  We are expecting transparency.  As an auditor, my goal is to confirm that the trial is run in a way that ensures the safety of subjects, protects their rights, and generates reliable data.  Sponsors want to continue working with sites in which so much effort has been invested and will work to identify areas for improvement if deficiencies are noted.  An inspector has a similar goal with respect to the assessment of trial conduct.  So, how do we ensure that trials are run at the level of quality that regulators are looking for and that are truly inspection ready?
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