Clinical trial recruitment solution: Get the right participants for your clinical research study easier and faster than ever before.

Discover why more life science teams are using OpenClinica Unite™ to automate source data acquisition from patient medical record systems to clinical trial research databases and case report forms.

As trial durations continue to grow, mid-study migrations are transforming from rare occurrences into a critical strategy for maintaining efficiency and data integrity in clinical research.

eConsent is transforming clinical research sites by addressing key pain points and streamlining processes for overburdened staff.

Here we highlight key advantages of EHR-to-EDC eSource, such as cost-effectiveness and improved site satisfaction.

Find out how OpenClinica stands out in the global EDC landscape through it's user-friendly interface, strong integration capabilities, and extensive partnerships.

Explore an EHR-to-EDC integration solution that enhances clinical trials by automating data transfer by bypassing manual data entry, reducing errors, and boosting efficiency.

This study summary highlights the improved accuracy and efficiency of automated data capture utilizing SMART on FHIR integration.

This panel discussion from the 2023 SCDM Annual Conference showcased the benefits of EHR eSource integration.

Manage some of the biggest pain points associated with site performance monitoring with an efficient reporting module that features powerful business intelligence reports for clinical trial management.

To gain a deeper understanding of successful study design, this article explores study personas, core design, a seven-step process for post go-live (PGL) changes, and more.

Clinical trial audits are evolving. Learn how transparency and efficiency can revolutionize the process, saving time and providing a deeper understanding of operations.

Uncover this groundbreaking automated study calendaring system, designed to revolutionize clinical trials by streamlining scheduling, enhancing user engagement, and ensuring timely data collection.

Interest in clinical trials is rising, with more people willing to participate. Here are four ways to strengthen patient engagement and enhance their experience in clinical research.

See how the implementation of cross-form logic can minimize data errors and alleviate burnout for clinical research coordinators handling complex trial data entry.

Discover the transformative power of EHR eSource integration through the eyes of a clinical research coordinator and project director in an adaptive platform trial.

Delve into the nuanced disparities between medical device and drug clinical trials with eight critical differentiators shaping regulatory pathways and patient safety.

Oncology clinical trials pose unique challenges. Dive into five key reasons behind the intricacies of oncology trials, from recruitment hurdles to data volume and efficacy endpoints.

Unlock the power of decentralized clinical trials with an electronic data capture platform (EDC). Discover how stakeholders benefit and what to consider when choosing the right EDC system.

One of the biggest risks for medical products and companies is the failure to report adverse events. But what leads to underreporting? Here are five core reasons behind most adverse event underreporting.

Discover the latest insights and trends shaping the landscape of clinical trials, like SMART on FHIR, patient-centered trials, eSource, and eConsent, with OpenClinica's most popular blogs of 2023.

Discover the power of EHR eSource in 2024—unlock 10 compelling reasons to elevate your approach and enhance clinical research outcomes.