Learn About Elomar History
About Us
Who We Are
Transforming Clinical Trials Through Innovation
Elomar Technologies is a dynamic startup founded in 2022 with a clear vision: to revolutionize the healthcare industry through cutting-edge digital solutions.
Our journey began with the development of DYD, an advanced eDiary solution designed to give our clients complete control over diary design and operations. Since then, we have expanded our vision, continuously innovating to provide efficient, compliant, and cost-effective software solutions tailored to the clinical trial ecosystem.
Today, we go beyond eDiaries—our growing suite of tools includes custom software solutions, an upcoming eConsent system, and an eCRF module. Every solution we create is designed to reduce dependencies, increase efficiency, and provide full regulatory compliance, ensuring that clinical trials run smoothly and cost-effectively.
With a commitment to empowering Sponsors and CROs, we provide not just software, but a strategic partnership to enhance trial management, streamline processes, and drive industry-wide progress.
We are more than just a software provider—we are a partner dedicated to transforming clinical trials into streamlined, controlled, and cost-efficient processes that meet the highest quality standards.
Our Core Values
in Clinical Trials Ecosystem."
01
Independence
Reducing reliance on third parties, fostering self-sufficiency in trial management.
02
Efficiency
Streamlining processes to optimize workflows, enhance productivity, and reduce costs.
03
Transparency
Know About Us
These Are Our Commitments
“Revolutionizing Clinical Trials Through Economically Empowered Clients.”
Cost Efficiency
Providing economic solutions that minimize trial expenses while maintaining quality.
Precision Control
Ensuring meticulous oversight of trial design, implementation, and execution.
Regulatory Excellence
Guaranteeing built-in compliance with FDA and EU regulations.
Continuous Evolution
Delivering a dynamic, ever-improving product that adapts to client needs.
We’re committed to empowering clinical research with innovative technology, seamless collaboration, and tailored solutions.
Whether you're looking for a strategic partner or simply want to learn more about what we do, let’s connect.
Have Any Doubts?
Questions And Answers
Can your e-diary run on any device?
Absolutely! Our e-diary follows the BYOD (Bring Your Own Device) principle, ensuring seamless access from any device.
Do I need experience in software requirements gathering?
Not at all! We guide you through every step to make it seamless.
Can I use your tool independently?
Yes! Our platform is fully self-service, but we’re always here to assist whenever needed.
We’re a small company. Can we afford your products?
Definitely! Our flexible pricing adapts to companies of all sizes, ensuring affordability without compromise.
Is your e-diary compliant with regulatory standards?
Yes! Our solutions are fully compliant with FDA 21 CFR Part 11 and EU regulations, ensuring secure and compliant trial management.
Can I customize the e-diary to fit my trial needs?
Absolutely! Our platform offers full flexibility, allowing you to tailor every aspect to your requirements.