Metrics-driven PM approach with customized collaboration and operational excellence for trouble-free clinical trials.
Eliminating barriers in study site selection and patient’s recruitment.
Custom-made, personalized support and full compliance with worldwide regulatory requirements.
We offer our global clinical monitoring capabilities in either a full-service or on a modular base.
We focus on the clear translation of the protocol into CDISC-compliant data structures with efficient data validation, review and management tools.
Reliable accuracy till the last page with proactive and efficient management of critical study documentation with technology-enabled TMF solutions.
Accelsiors’ safety team offers medical expertise and patient safety support across all geographic regions.
We provide improved compliance, study performance and reliable results with our holistic Quality Management System.
Our biostatisticians facilitate the success of clinical research in a significantly regulated environment.
Working closely with DM, statistical, medical, regulatory and safety teams, our medical writers deliver high quality reports with high scientific and industry standards.
Accelsiors ensures efficient and smooth management of third-party vendor partnerships including central or local labs and global drug supply management.