Best Clinical Trial Management Systems - Page 6

Delve Health

Delve Health is a clinical trial compliance and patient engagement company. We combine eCOA/ePRO, wearable device integration, real-time analytics, and Concierge-as-a-Service™ to help sponsors, CROs, and research sites run studies with higher completion rates, stronger retention, and cleaner data. Based in Minneapolis, serving programs across North America, Europe, Asia, and MENA.

DFdiscover

diCELLa eCRF clinical trials

DiGenesis Platform

Diligent360

Diligent360 is an end-to-end Vendor management platform, built for the clinical trials industry. Diligent360 unifies the entire Vendor lifecycle from discovery and qualification through ongoing monitoring, so you can reduce delays, make risk-based decisions, and stay ahead of evolving compliance demands.

EasyTrial

EasyTrial is a Clinical Trial Management Software. EasyTrial is perfect for optimizing the time you spend managing visits, patients, booking etc. by keeping all data in one place and by giving a clear overview. Enjoy features like automatic reminders and 100% customizable eCRF creation.

eCaseLink CTMS

eClinDirect, DSG’s web-based CTMS, is a project management application that helps you to capture and share a wide variety of clinical trial project status information across multiple studies.

eClinPro CTMS & eSource

eCooperate

With our strong continuation capabilities, Taimei Technology CTMS (eCooperate) can seamlessly integrate into your existing processes and workflows, allowing you to customize the system to fit your unique needs. Whether you're managing a single-site study or a complex, multi-site trial, our platform can be tailored to your specific requirements.

eCTMS

EDETEK BioStat.AI

EDGE Clinical

EDGE is an innovative cloud-based research management system created by the Clinical Informatics Research Unit at the University of Southampton.

ekomite

Elips'PHARMA

elsai Clinical Protocol Audit Agent

elsai Clinical Protocol Audit Agent helps sponsors, CROs, regulatory affairs teams, compliance specialists, and medical writers review clinical study documents with greater consistency, traceability, and control. The agent evaluates protocols, informed consent forms, recruitment materials, and other clinical study documents against configurable validation and compliance rules. Instead of returning unsupported findings, every issue must be backed by exact source text from the document. If supporting evidence cannot be verified, the finding is excluded. For each validation rule, the agent identifies the relevant section, verifies the underlying evidence, determines whether the document meets the requirement, explains the reasoning, and provides a confidence score. Where appropriate, it can also recommend corrected or replacement text for human review.