Clinical Data Miner
The data backbone of the IOTA consortium
Clinical Data Miner is a mature, ultrasound-focused clinical data capture, curation and research platform built with and for the IOTA consortium.
Who CDM is for
For study leaders and contributors.
Existing users can access CDM directly at cdm.gynaia.com. If you are joining a study, visit iotaplus.org to register your center and link your research project. If you are interested in starting a study, connect with info@gynaia.com.
For research institutes.
Hospitals and research groups setting up new studies can use CDM to build structured imaging and clinical databases for gynecological, obstetric, or fertility studies.
For technology developers.
CDM hosts the world’s richest data collection in gynecological oncology. We collaborate with vendors, academics, and algorithm developers on multi-center validation studies.
Collect & curate structured, real-world evidence
CDM supports standardized collection and curation of imaging and clinical data and currently serves more than 40,000 cases, 200 centers, and 30 countries.
CDM underpins the data infrastructure for major IOTA and IETA studies, enabling reproducible research, validation of diagnostic models, and real-world evidence generation in gynecologic ultrasound.
Managing studies with precision
Gynaia provides an end-to-end data platform for clinical studies, from daily data submission, collection, and curation to study design, form setup, and multi-center coordination.
We provide the tools for data cleaning, monitoring, and quality assurance to ensure every dataset is structured and analysis-ready.
We also collaborate with vendors, academics, and algorithm developers to validate models, assess medical device performance, and conduct retrospective analyses in women’s health.
Designed for real clinical research.
Your questions, answered
What is Clinical Data Miner (CDM)?
CDM is a data management platform built for gynecological and ultrasound-based clinical studies, supporting standardized data collection, curation, and analysis.
Who can use CDM?
IOTA consortium members, study leaders, and partner institutions conducting research in women’s health.
Research institutions wanting to set up their own studies.
Validation partners wishing to conduct a multi-center validation study.
How do I access CDM?
Existing users can log in at cdm.gynaia.com. New users can register or join a study through iotaplus.org. Prospective partners can reach out to info@gynaia.com.
Can CDM be used for new studies?
Yes. Gynaia helps hospitals and research groups configure new multicenter studies, including forms, workflows, and monitoring.
Can CDM support AI or algorithm validation?
Yes. Its structured datasets are ideal for model training, testing, and regulatory validation in women’s health.
Is CDM only for IOTA studies?
No. While developed within IOTA, CDM can support any gynecology, obstetrics, or fertility research project.
Get Started with Gynaia
Improve patient outcomes with learning & development, quality assessment, and clinical decision support.