We are dedicated to the management and execution of centralized and decentralized clinical research studies.
We eliminate inefficiencies, accelerate user adoption and improve productivity from study startup to closeout.
We provide unified study management services leveraging our curated processes for multi-site clinical studies.
Our state of the art technology and cloud platform helps simplify and manage the complexity of all regulatory activities.
We look forward to hearing from you and your team!
We enable you to accelerate research and help everyone live healthier lives.
We are a team of research professionals who constantly innovate and strive to improve timelines, quality and productivity of research outcomes. We work with research sponsors, sites and organizations to successfully manage all regulatory requirements.
to take research to a new level, are you ready?
We offer comprehensive unified study management services for multi-site clinical research studies
We connect research sponsors and sites using our secure cloud based platform and unified services
We simplify complex regulatory documentation and create easy to use workflows for research teams
All users are provisioned and trained by our rapid on-boarding process. Most sites are functional in weeks
Our managed eRegulatory services help stakeholders achieve research regulatory requirements
We streamline research processes, create workflows and increase research efficiency
We proactively reduce manual processes, eliminate inefficiencies and costly errors
Your data is compliance and audit ready for FDA CFR 21 Part 11 with automated audit trails
We provide effective oversight and quality assurance of all regulatory requirements
We perform secure archival of study documentation, data records and restrict access control
We look forward to hearing from you and your team!
Our purpose is to improve research timelines, reduce operational costs, increase quality and enhance compliance requirements.
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