EvidentIQ Group designs and operates purpose-built software to support the full lifecycle of clinical research. Our platforms enable pharmaceutical, biotech, and research organisations to run efficient, compliant, and data-driven clinical programmes, with built-in GxP and 21 CFR Part 11 controls. We integrate practical AI into core clinical workflows to improve data quality, reduce manual effort, and support reliable decision-making driving progress that matters.
EvidentIQ Group brings over 20 years of clinical research experience to the design and development of eClinical software. Our solutions are purpose-built to adapt to study-specific requirements and regulated workflows. They improve data accuracy, streamline processing, and increase efficiency across clinical operations.
EvidentIQ Group is a portfolio of digital platforms designed to address the scientific, operational, and regulatory demands of modern clinical research. Each platform supports a defined stage of the clinical research lifecycle while adhering to consistent standards of data integrity and regulatory compliance.
Dacima delivers a highly configurable Electronic Data Capture platform for complex study designs and regulatory-driven data collection. Clindex supports clinical trial operations through integrated data capture, oversight, and workflow coordination. Carenity extends these capabilities by enabling direct patient engagement and real-world evidence generation through established patient communities.
Our platforms allow organisations to define the appropriate level of flexibility, integration, and patient involvement for their clinical research strategy, while maintaining scientific rigor and compliance across studies.
Founded 2006 in Canada
Why Dacima
Founded and developed by experts in epidemiology, medical research, and information technology, Dacima meets the regulatory and operational requirements of modern clinical research while enabling flexible study design and reliable data management.
Dacima Customer groups
Primarily used in the USA and Canada with a Focus on CROs, Biotechs, Academics and NGOs.
Founded 1997 in USA
Why Clindex
Clindex is designed for organisations that require complete oversight of clinical trial data across EDC, CTMS, eTMF, and eCOA/ePRO within a single platform. It is well suited to studies that demand configurable workflows, advanced administrative control, and non-standard data collection models.
Clindex is particularly effective for complex operational settings such as Phase I units, diagnostic organisations, and imaging core laboratories, where study execution and data oversight must be tightly coordinated.
Clindex Customer Groups
Primarilyy used in the USA with a focus on Medical Devices, Diagnostics, Biotechs, Imaging Core Labs, CROs and Phase I Units.
Founded 2011 in France
Why Carenity
The platform provides compliant, direct access to thousands of patients worldwide across more than 1,200 diseases and has contributed to over 500 scientific publications and studies.
Carenity Customer groups
Carenity collaborates with the life sciences industry (pharmaceutical, biotech/medtech and medical devices companies), academics, patient advocacy groups, CROs and consulting firms.
Carenity leverages real-world patient insights to bring value at each stage of the drug life cycle: clinical development, market access/HEOR, RWE, Medical Affairs and Commercial.
Our Commitment to shaping the future of clinical trials
At EvidentIQ, we develop scalable and flexible solutions that keep our clients at the forefront of the constantly evolving clinical research industry. Our platform is designed from the ground up to seamlessly integrate with other systems, providing deeper insights for faster, more informed decision-making.
We commit to continuous innovation, by expanding and evolving our platform with cutting-edge solutions that effectively harness vast amounts of data to build actionable intelligence that will drive forth the future of clinical research success and clinical data management.
EvidentIQ Group follows a modular systems approach, allowing organisations to combine EDC, clinical trial management, and eCRF capabilities within a single secure platform. This structure supports tailored system configurations while maintaining consistent standards for data quality, operational oversight, and regulatory compliance.
Supporting leading pharma companies and CROs worldwide
