Highly Qualified Monitoring is key to obtaining reliable results, the most important outcome of an expensive clinical trial.
Monitoring is a significant cost factor of a trial that can be minimized by effective monitoring based upon a good monitoring plan. Our experience in risk based and adaptive monitoring, acceptable to the regulators and authorities, can be a valuable component of a cost effective plan.
Our trained clinical research associates (CRAs) are experienced at communicating with sites in a well-respected and effective way to ensure high quality of data and fast resolution of problems. They have experience working for international sponsors and performing professional site initiation, on-site monitoring and close-out visits.
Our CRAs can offer special support for inexperienced sites to ensure procedures are performed according to GCP.