DIA GLOBAL

Our eClinical solutions simplify and automate clinical processes, enabling sponsors, CROs, and sites around the world to expedite timelines, enable collaboration, improve quality, capture the full story of study, and pass inspections.

Our eCOA migration process is designed to ensure conceptual equivalence and cultural appropriateness in any language, minimizing time-to-market, mitigating risk, and ensuring regulatory compliance in global studies.

We simplify the complexities of the regulatory environment, avoiding critical errors and regulatory roadblocks. Seamlessly complete global submissions, clear regulatory hurdles, and shorten development timelines in your submissions process.

GlobalLink, our global translation management system, simplifies the entire translation process from submission to release, managing review processes, and maintaining audit trails to deliver improved translation quality.

We leverage artificial intelligence and machine learning capabilities to help our clients meet their goals by combining best-of-breed neural machine translation (NMT) with best-practice approaches for optimizing content and business processes.

Comprehensive solutions  for observing, detecting, and monitoring the effects of your pharmacovigilance products across locations and languages through local literature monitoring, case triage, redaction support, and translation.

Empowering omnichannel communications with technology-backed workflows to assist with content, localization, and management of medical affairs content. Improve day-to-day operations and reduce administrative burdens with our suite of solutions, including Medical Writing, Content Reuse, Call Center Support, and more.

Our AI-powered eTMF empowers every stakeholder – from study managers and CRAs, to IT teams and business leadership – to be more compliant. Speed timelines and maintain TMF health through automation workflows with machine learning to make inspection readiness easier than ever with 98% accuracy.

Tackle the challenges of clinical operations with a mobile-first clinical trial management solution focused on CRA monitoring. TI CTMS enables remote oversight and powerful interoperability with site feasibility, study start-up, eTMF, LMS, content management, and collaboration.