Clinical inspection readiness perspectives: CRO vs Sponsor

Pharma IQ
Posted: 07/14/2017

If your company was handed with a notice for a clinical trial inspection right now, what would the reaction be?  A feeling of calm confidence or a rush of slight concern? In this ebook Pharma IQ compared the perspectives of a Clinical Research Organisation (CRO) to that of a sponsor concerning the burning topic of trial master file inspection readiness.

Interested in learning more about this topic?
TMF agenda
Download The Brochure for Trial Master File Europe 2017 Here

As one of the most heavily regulated industries in the world, the success of clinical research relies heavily on accurate documentation and data management. Collating and maintaining well organised, accurate documentation that is easy to access and inspect is harder than it sounds. Download the agenda for the Trial Master File and Inspection Readiness Summit here. 

Need some tips? Take a look at our interactive inspection ready infographic featuring intel from the MHRA's Senior Good Clinical Practice Inspector Andy Fisher. 

                   inspection ready

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Pharma IQ
Posted: 07/14/2017

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