Trial Interactive offers a variety of solutions and services that accelerate the processes associated with global product development and provide critical subject matter expertise and scalable resourcing on demand.

Our experienced staff will assist you with fast, 24/7 support. Our range of solutions includes:

TMF Services

Comprehensive TMF management services help study teams establish best practices, process TMF documentation, and stay inspection ready. Scale your study team anytime, anywhere around the world.

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.

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.