Cytespace provides support to pharmaceutical/biotech/ medical device companies in planning the required analyses before the study begins and offers expert input to essential documents as the study progresses. Aiming to optimize your clinical development strategy, our expert consultants develop the innovative strategies and capabilities needed to launch products with the greatest potential for commercial success and patient outcomes. Whether you have focal needs or search a broad set of solutions for your development program, you may count on our experts, to ensure the biostatistical, medical and regulatory aspects of the program, along with its market perspective, are consistent with your goals. We do coordinate with the medical writing team to identify the best clinical trial design (Like Adaptive Clinical Trial etc.), prepare randomization, statistical analysis plan, TLFs and statistical reports.