EDC Resources
-
The Evolution Of The Modern Medical Monitor
6/26/2020
How to identify, hire, and empower a modern medical monitor to help your next study proceed toward submission more productively, and with greater data integrity, than ever before.
-
How Heron Therapeutics Sped Up Database Creation
12/2/2022
Electronic data capture (EDC) is straightforward, in theory. However, not every EDC is purpose-designed for ease of use by study teams, and some are easier to use and more intuitive than others.
-
Efficiently Manage Clinical Data With Castor's EDC, CDMS
5/11/2023
Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.
-
Broadening Eligibility Criteria Among Cancer Clinical Trials Patients
9/17/2024
This study challenges the commonly applied exclusionary approach to clinical trials, particularly cancer trials, that underrepresent certain populations and limit the generalizability of research advancements.
-
The Future Of AI Analytics On Chronic Pain And Neurological DHTs In Clinical Research
5/27/2025
This presentation explores how DHTs and AI-driven diagnostics are transforming clinical research, supporting more accurate assessments and accelerating therapeutic development in chronic pain and neurological disorders.
-
Site Satisfaction: Influencing Tech Development Strategies
4/19/2023
Technology is playing an increasingly important role in clinical trials, helping to improve efficiency, compliance, and data quality. Learn why it’s critical that clinical study technologies are easy to use across sites and fit into the team’s workflows.
-
Speeding The Switch To Risk-Based Monitoring
8/30/2017
The adoption of RBM is increasing as companies provide greater management support, staff training and more sophisticated technology systems. Technology platforms that enable continuous monitoring with near real-time intuitive visualizations, analytic dashboards and applications will allow issues to be identified and addressed early, improving study safety and efficiency.
-
Simplifying The Vineland-3: Assisting Raters, Reducing Burden, And Improving Data Quality
10/21/2024
Electronic versions of both Vineland-II and Vineland-3 have been developed with features to improve data accuracy and consistency such as built-in prompts, item-specific scoring guidance, and automated calculations.
-
Our Unified Platform Serves As eSource For COVID Treatment Trial
6/17/2024
Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.
-
Adapting To The Medical Monitor: Driving Tech Adoption In Clinical Analytics
7/7/2020
Reasoning for physician monitors’ reluctance, and what technology needs to offer to convince monitors their work can be more efficient: quickly detecting safety signals and speeding time to submission.