Eudract Trial Summary posting

Innovion provides expert services for posting the Clinical Trial Summary results into the Eudract system. Since 21 July 2014, it is mandatory for sponsors to post clinical trial results in the European Clinical Trials Database (EudraCT), managed by the European Medicines Agency (EMA).

Eudract 1Innovion offers a fast and flexible solution to ensure compliance within the defined timelines. Over the past years, an expert team has developed a standardized and partly automated routine to deliver this high-quality service.


Most Eudract postings requires manual data entry, which is not cost-effective and error prone. However, a substantial part of the trial summary data can be submitted by uploading an XML file. Where possible, Innovion uses XML files to upload the trial summary data.

About Innovion

Innovion aims to translate clinical data needs into sustainable solutions.

Zoetewei 118, 2580 Putte - Belgium

+32 476 545 917 |

A passion for data

We are passionate about the value of data. We love a complex challenge and deliver pragmatic, innovative and cost-effective solutions. We are convinced that efficiencies will be gained through data standardization. Expect a customer oriented service and our strong belief that success is built on partnerships.

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