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Updated: Aug 31, 2026

Monitoring Kinase and Phosphatase Activities Through the Cell Cycle by Ratiometric FRET
Published on: January 27, 2012
[From start to finish - Responsible reporting of clinical trials at Karolinska Institutet]
Sofie Possmark1, Cecilia Martinsson Björkdahl2
1med dr, samordnare, avdelningen för forskarstöd (RSO), Karolinska institutet.
Abstract:
In the autumn of 2020, Karolinska Institutet (KI) began the process of centralizing the registration and results reporting of clinical pharmaceutical trials. Up until that point, KI had not reported results for any trial in EudraCT, which is required by law. In response, two full-time employees were recruited to contact researchers and provide hands-on support in uploading their results to the portal. As the EudraCT portal can be perceived as non-user friendly, clear guidelines were written, and a webpage developed to make information more accessible. The response from researchers has been positive. However, the shift to centralization has required a considerate amount of work for KI staff. In addition, motivating researchers to upload old trial results is challenging, particularly if they are not responsive or are no longer employed at KI. Therefore, it is crucial to have support from management for investment in long-term solutions. Currently, the results reporting for completed trials at KI has increased from 0% to 61%.
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