Towards an optimal clinical trial process...
and healthcare costs.
Improving efficiency may not always yield the best results, as it can have unintended consequences at other levels. Optimization is more inclusive and involves all aspects of the process, such as quality, requlatory requirements and making your data FAIR (Findable, Accessible, Interoperable and Reproduceable). Our professionals help you with this process. This includes designing processes and solutions, addressing stakeholder concerns, picturing your future data processes, change impact analysis and more. We work with different partners to get the best results for our customers.
ClinLine was founded in 2018 by Berber Snoeijer.
With a university degree in Biomedical Sciences and her varied and extensive experience in clinical trial medical writing, data management, data analysis and reporting, she oversees the entire clinical trial data process with all its complexities and is able to link this to trial design and clinical operations.
She owned a Clinical Research Organisation from 2001 to 2008, where she established and managed business processes, created solutions and standards to streamline work, and collaborated with her team on numerous phase 1 to phase 4 trials in various therapeutic areas. Following that, she worked as an R&D manager in a real-world data institute, unlocking the potential of real-world data and designing efficient and reliable tools for this purpose. In 2018, Berber founded ClinLine, which focuses on optimizing the clinical trial process as a whole. Drawing on stakeholder input and requirements, she provides input and designs for data structures, solutions, and process optimization.