TransPerfect Trial Interactive
TransPerfect Trial Interactive is a leading provider of web-based clinical trial, clinical development, product licensing, alliance management, and data room solutions that enable life sciences companies to collaborate on partnerships or clinical trials, streamlining time to study start up and reducing administrative burdens during the conduct of a clinical trial. Trial Interactive provides the ability to complete, maintain, and update clinical trial documentation in a secure online environment.
Companies will also benefit by being able to stay in compliance with FDA and other regulatory bodies' requirements for sharing and tracking safety data with study investigators participating in the clinical trial. Fast repository creation and 24/7 support help pharmaceutical, biotechnology, and medical device companies as well as CROs conducting clinical trials achieve cost and time efficiencies during the clinical trial process. With a SAS 70 Level II certified hosting environment, next-generation encryption, and intrusion detection, Trial Interactive allows customers to rest assured that their confidential clinical trial information is secure and protected. Founded in 1999, Transperfect Trial Interactive currently provides intuitive, web-based document repositories to over 13,000 professionals from more than 450 organizations on a global basis.
Global Clinical Trial Solutions
Trial Interactive offers a variety of software solutions and services to streamline and speed the processes associated with global clinical development, CRO outsourcing and management, biotechnology and pharmaceutical product licensing, and alliance management. Trial Interactive can streamline an array of functions including:
- Starting your investigator feasibility process
- Hosting your investigators' Essential & Regulatory Documents in a collaborative online repository
- Sharing access to investigative site Regulatory Binders or Study Manuals amongst your study teams
- Delivering safety reports to investigators
Whatever your need, our experienced staff will assist you through the process and provide fast, 24/7 support. Please follow the links below to trialinteractive.com to learn more about our range of multilingual clinical trial solutions:
- Biotech & Pharma Product Licensing & Alliance Management
- Biotech & Pharma Due Diligence
- Clinical Development Data Rooms
- Pharmacovigilance & Safety Reporting
- Global Multilingual Clinical Trial Support
- Essential & Regulatory Documents Completion
- Electronic Trial Master Files
- Collaborative Workspaces
- Clinical Development Document Management
- Electronic Regulatory & Study Binders
Contact one of our client service representatives at +1.212.400.8848 / Toll Free: +1.877.523.4888 to learn more.