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How our customer automated the analysis of scientific literature for the drafting of clinical evaluation reports (CER).
With ever-changing regulations, clinical data has become essential for the marketing of medical devices.
Our client, a firm specializing in the drafting of clinical evaluation reports (CERs), is helping manufacturers adapt to the new 2017/745 regulation.
This regulation has increased the requirements for rigor and transparency in CER writing, particularly with regard to bibliographic research.
These new requirements represent a challenge for CER writers, our platform offers specific functionalities to overcome them efficiently.