Comprehensive Clinical Development Services
Accelsiors offers a complete range of expertise in support of your specific needs: scientific, analytical and regulatory complemented by global resources, state-of-the-art technologies and project management methodology for the most effective execution of your development program across all phases of clinical drug development.
Full service CRO solutions
We provide you a team of subject matter experts to support, tailor and lead your study and advise you on the optimal directions from the study design to the delivery of high-quality results.
Our data science experts and the used state-of-the-art technologies will support you with insightful solutions in all aspects of handling and analysis of clinical study data across all phases of your study.
Our Global Regulatory Affairs team will help you to navigate through the maze of complex legal landscape around the world.
Comprehensive services to properly handle constantly moving elements of your first-in-humans and proof-of-concept studies
End-to-end suite of services for Phase II – III studies, focused on a rapid and professionally supported progress towards your drug’s approval, on-time, on-budget
Clinical development services
To find the well performing sites and the right patients is one of the most challenging steps in the life-cycle of a clinical trial.
With our pharmacokinetic / pharmacodynamic modelling and simulation we provide answers on efficacy and safety of new drugs faster and at a lower cost.
Proactive and efficient management of critical study documentation including compilation of the Trial Master File (TMF). Your data is our priority and ultimate deliverable.
We focus on the clear translation of the protocol into CDISC-compliant data structures, efficient data validation and review tools.
Effective Project Management is key in successful planning, execution and completion of complex studies throughout all phases of development.
Accelsiors provides compre-hensive clinical monitoring services in all key areas of drug development.
Accelsiors’ safety management team offers medical expertise and patient safety support to our clinical teams across all geographic regions.
Our biostatisticians facilitate the success of clinical research in a significantly regulated environment.
Working closely with data management, biostatistical, medical, regulatory and safety teams, our medical writers deliver high quality reports with high scientific and industry standards.
At Accelsiors we have quality built-in to all of our processes, everyone is responsible for ensuring quality delivery.
