Centrical can provide all levels of feasibility services ranging from high level country specific information relevant to your therapeutic area and trial through to detailed study and site specific data. It's your choice.
Our highly professional team has extensive clinical trial experience so we fully understand the consequences of poor site identification, including delays in study start-up, changes in sites and countries, budget increases and slow recruitment.
Feasibility done correctly allows for proactive analysis and management of timelines, subjects, study design and budget and builds the risk mitigation strategies into the planning process before the study is initiated. With the foresight to perform this type of feasibility planning, substantial value and return on investment may be realised.
As an independent company, our feasibility is focused entirely on identifying sites that map to specific study parameters and is not influenced by pre-existing outsourcing constraints.
For pharma and biotech our comprehensive systems and processes allow us to operate globally and to provide web-based access to your feasibility information in various different formats.