We provide services within statistics, data management (DM), clinical research (CR), pharmacovigilance (PV) and data monitoring committees (DMCs). We can assist you in planning and managing all phases of your clinical trials; from initiation (e.g. clinical development plans, feasibility and patient recruitment) and conduct (e.g. data handling monitoring and document management) to close-out and finalization (e.g. close-out visits, statistical analysis and reporting).
Kategorier: Life Science Consultants