Reclamation Projects

Clinical Trials requiring corrective action often cause the Client to pay double for completed data; once for the initial, inadequate monitoring and processing, and again for reclamation efforts and expertise.  In addition, the Client frequently pays a higher rate for reclamation services in order to be assured of the appropriate level of expertise required for bringing the project into compliance with FDA CFR, ICH, GCP Guidelines, and corporate SOPs, policies and procedures. 

Principal Investigator(s) and Client staff are generally less satisfied when required to repeat work previously completed. Frequently placed into uncomfortable situations, our reclamation staff is experienced and extremely proficient in utilizing operational expertise, while working to resolve the most complicated issues.

To help our Clients avoid the pitfalls of painful and expensive reclamation services, RESQ emerged as an FSP to support clinical trial development with services provided by only senior level industry experienced staff, and at fair and reasonable rates.  The individuals who provide RESQ’s reclamation services are the same professionals who work as Trial Monitors, Project Managers, CRAs, Medical Writers, Clinical Data Managers, Statisticians, and Quality Auditors to ensure Client projects are routinely compliant, from project initiation onward.