Clinical documentation is the process of gathering data from clinical studies. Medical device manufacturers must ensure their Clinical Evaluation Report is accurate and up to date. This regulatory process may seem complex, but it aims to improve patient safety. Manufacturers must gather as much data as possible to ensure high-quality CERs.
LTTS aids manufacturing companies with their CER requirements. With extensive experience with CE regulations, LTTS can provide them with a customized solution for clinical literature reviews to meet CE regulations. A streamlined and optimized workflow compliance program can be set up by LTTS for medical device companies. Our experience in managing compliance programs and automating them allows us to make the process as efficient as possible.