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Trial Master Files & Inspection Readiness

Trial Master Files & Inspection Readiness

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. Moreover, inaccurate clinical data and critical findings have significant budgetary implications. This puts a lot of pressure on clinical operations teams and TMF owners.

Pharma IQs TMF & Inspection Readiness conference is designed to help ease this pressure and will provide the insight attendees need to perfect their TMF, and achieve constant inspection readiness.Location: Amsterdam, Netherlands

Meeting Dates: June 18-22, 2017

Exhibit Dates: June 18-21, 2017

Montrium will be showcasing its full suite of Document & Quality Management applications as well as its Connect Platform. To learn more about our industry-leading enterprise content management solutions, drop by our booth to speak to the team.