Where Simple Meets Powerful.

Manage your clinical research site, site network, CRO, or sponsor data with intuitive software systems and unmatched customer service.

SITES & NETWORKS

Try one system or bundle them all for a complete Site Operations Management System (SOMS)

SPONSORS & CROs

Maximize efficiencies, improve trial management, and reduce costs.

0
STUDIES
0
SITES
0
PATIENTS

Your success is our success

Top rated CTMS on Capterra!

Request a Free RealTime DEMO

THE REALTIME FAMILY OF BRANDS

Complion

Connecting Investigators & Sponsors to Compliance

Eliminate paper and redundancies as well as ensure on-demand monitor-readiness with top-tier eRegulatory/eISF solutions designed for ACMs, Sponsors, and CROs.

Accelerating Clinical Trials through Power of Data

Boost study success with the industry’s leading solution for pipeline management, study startup, metrics capture and intelligence – your key to site performance improvement.

View study documents, refer patients,
sign documents with your fingerprint and more!

BLOG: BEHIND THE SOFTWARE

Improving Patient Engagement & Retention Strategies

Improving Patient Engagement & Retention Strategies with ENGAGE!  

Maintaining patient engagement and minimizing dropout rates in clinical trials is a persistent hurdle, with dropout rates soaring up to 30% in some studies. The National Institutes of Health underscores the importance of building trust, engaging communities, and ensuring clear and culturally sensitive communication at every stage, from pre-recruitment planning to post-study dissemination of results.

Read More »
What is a CTMS

What is a Clinical Trial Management System (CTMS)?

Clinical trials are fundamental in advancing medical science, offering new treatments and drugs to improve patient care. However, managing these trials is a complex task involving multiple stages and stakeholders. To streamline this process, Clinical Trial Management Systems (CTMS) have become essential for clinical research sites to organize efficient site management.  Historically, clinical trial management

Read More »
What is eSource in Clinical Trials?

What is eSource in Clinical Trials? Beyond Paper. 

Technological advancements and adoption in clinical trials continue to reshape the way data is collected, managed, and analyzed by clinical research sites, sponsors and CROs. Over the last decade, Electronic Source (eSource) has gained prominence for enabling direct data entry by investigators, reducing transcription errors and enhancing data quality.   eSource in clinical trials is often

Read More »