The highly competitive and regulated world of drug research and development is experiencing a digital transformation.  Traditional methods of managing clinical trial documentation are being replaced by more effective and efficient electronic technologies.  Whether your organization is seeking to transition from paper to electronic document management, reduce a large document backlog, or are prepare for an upcoming inspection, Sentinel Clinical Solutions can assist with all aspects of the records management process. Through our focus on regulatory inspection readiness, we provide a wide range of services that help organizations achieve operational excellence and regulatory compliance. 

With over a 10 years of experience in clinical operations, we understand the challenges facing small and mid-sized companies. Resources are often limited and timelines are critical, so our team will guide you through developing processes that are regulatory compliant and right-sized for the resourcing capabilities of your organization. 

Our pragmatic, risk-based approach to TMF management is designed to ensure compliance. Much more than a checklist of required records, we implement innovative processes that allow you to face regulatory interactions with confidence. Whether your needs are temporary or long term, Sentinel Clinical Solutions is a committed partner, working alongside your team to and allowing you to focus on critical aspects of the trial management.