Trial Interactive offers a variety of e-clinical solutions and services which accelerate the processes associated with global clinical development, CRO outsourcing and management, biotechnology and pharmaceutical study start-up, pharmacovigilance and safety reporting, electronic Trial Master File, product licensing and alliance management, and more.

Whatever you need, our experienced staff will assist you through the process and provide fast, 24/7 support. Our range of solutions includes:


Trial Interactive's e-feasibility streamlines the global feasibility process for deciding which countries should be in a study based on the disease prevalence, access to patients, regulations, and more.

Electronic Investigative Site Files (eISF)

Managing the investigative site files (ISFs) has traditionally been a labor-intensive, paper-based, manual process for sites, sponsors and CROs.

Learning Management Systems (LMS)

LMS or Learning Management Systems have widely been adopted to host training materials and streamline the global training of staff for companies.

Study Start-Up

One of the many challenges in conducting clinical trials is the speed to completion and finalization of essential and regulatory documents by the investigative site personnel. Trial Interactive makes the process more efficient by integrating our Study Start-Up module with our eTMF.

Electronic Trial Master Files (eTMF)

With today's technology, centralized global access to TMF documentation is readily available to study teams and complies with regulatory authority requirements.

Clinical Development Document Management

TransPerfect's global document management capabilities allow rapid scanning, coding, and indexing of development and commercialization documentation.

Global Clinical Trial Support

Trial Interactive client services personnel have a deep understanding of the clinical development industry and provide consultative assistance with a focus on meeting your organization's objectives.

Pharmacovigilance & Safety Reporting

Rapid collection of cases into Trial Interactive allows prompt case assignment and review as required by regulatory authorities to protect patient safety.

Global Multilingual Call Center

TransPerfect's staff, whether healthcare professionals or medical interpreters, can receive and process calls in over 170 languages.

Endpoint Adjudication

Trial Interactive provides a collaborative work space for all relevant stakeholders – including investigative site personnel, core labs, and study teams – where these cases can be collected and delivered to adjudicators.

Institutional Review Board (IRB) Solutions

Whether you are a central IRB in North America or an IRB or Ethics Committee affiliated with a hospital, Trial Interactive has the ideal solution to streamline your processes.

Global Product Launch

In the life science industry, launching a new product is always a challenge. The process becomes even more complicated when launching the product globally. For over 20 years, TransPerfect has assisted life science companies with global, regional, and country level product launches.

Electronic Regulatory & Study Binders

Trial Interactive offers a complete solution for electronic distribution of essential documents and other sponsor and/or CRO forms that need to be completed. All information can be completed virtually, resulting in a paperless process.

Central Laboratory Solutions

Trial Interactive has assisted many central laboratory providers in removing the need to express-mail documents, and we provide real-time access to user activity. Knowing that your investigative site staff reviewed the critical laboratory reports allows you to rapidly improve regulatory compliance.

Due Diligence

Companies that are participating in licensing activities can securely share confidential product development information through an easy-to-use, web-based platform with Trial Interactive.

Clinical Outcome Assessment (COA) Management

Trial Interactive creates a scalable solution to securely manage Clinical Outcome Assessments and all related documentation, increasing efficiencies in the clinical development and trial processes while giving a secure visibility to all stakeholders.