We can manage all aspects of your clinical study including Project Management, Regulatory, Biostatistics, Site Selection and Feasibility, as well as eCRF design and configuration.

We have a complete team of global CRAs and Lead CRAs providing Quality Control Visits as well as Co-Monitoring Visits and more.

Our Medical Monitoring Team can manage all of your Safety and Pharmacovigilance needs including Safety Management Setup, AE / SAE Case Processing, Safety Narrative Writing and Safety Report Submissions.

Our Auditors can tackle all of your auditing requirements including Auditing of Sponsors, CRO's and Vendors, Compliance Audits and Project Audits.