Clinical Trial Data Solutions
Innovative software for efficient analysis and reporting in pharma.
Clinical Trial Data Solutions
Innovative software for efficient analysis and reporting in pharma.
About Clinovate
Our Mission
We are committed to developing software that fully complies with FDA 21 CFR Part 11, GCP, and ICH guidelines. Our approach adheres to industry best practices for validated and well-documented systems, incorporating robust audit trails and access controls to ensure data integrity throughout the software lifecycle.
Efficiency and Innovation
Our advanced standardized solutions are tailored to harness the power of SAS, R, Generative AI, and Automation, enabling research organizations to innovate and drive growth.
Compliance and Support
Our software is fully compliant with CDISC standards for SDTM and ADaM datasets, and is aligned with FDA guidelines for the generation of tables, listings, and figures (TLFs). Quality support is integral to our services. We offer dedicated assistance, training, and ongoing guidance to ensure that our clients maximize the value of our software solutions.
Contact Us
Questions or Comments?
We know that our clients have unique needs. Send us a message, and we will get back to you soon.
