In consideration of the study, ClinActis will assign locally-based CRAs in the individual countries, who are familiar with their country regulatory requirements and ideally with previous experience monitoring global international clinical trials.
Training and Cultural Knowledge
Our clinical monitoring teams are well-equipped to deliver fast, efficient investigator site support and data oversight for your study. ClinActis requires our CRAs to demonstrate proficiency in site monitoring before being allocated to a study and are mainly assigned to monitor sites in their home countries which provides the necessary understanding of local languages, regulations, customs and business practices.
Accelerate Database Lock
Since ClinActis prepares our CRAs with study-specific training and who are familiar with local customs and regulatory requirements, this training and cultural knowledge improves site workflow management, reduce investigator burden, improve data quality and accelerate the database lock.