PURE, NNIT’s comprehensive clinical trial registry, lets you effectively manage clinical trial data while keeping up with changing requirements.
PURE fulfils the life science industry’s need for an effective and state-of-the-art solution to manage trial information while keeping a promise of transparency to patients, doctors, internal staff and other stakeholders.
In short, with PURE you’re in control, compliant, and on schedule.
Stay in control throughout the entire clinical
With no central IT system in place, consistency, accuracy, and effective data communication are at stake. PURE serves as a back-end system and a portal to store, access, and control clinical trial data at every stage of the process, across the company.
Stay compliant with FDA Amendments Act (FDAAA)
PURE makes sure all approved clinical trial data is compiled and accessible in a way to comply with current and future FDA requirements.
Stay on schedule at ClinicalTrials.gov and EudraCT
PURE handles the full process flow for internal approval, export and registration of clinical trials to ClinicalTrials.gov. In the near future, trial registrations at EudraCT will be included in PURE as well.
Read more about how PURE can help your company.
