Clinical Development Data Rooms

User-friendly design, combined with optimized technology for high-speed document transfers make Trial Interactive data rooms a simple, secure, streamlined solution for the clinical trial process. TransPerfect data rooms enable you to securely host clinical trial-related documents online for your clinical study, significantly speeding up trial processes while extending your reach to your study investigators and other stakeholders in the your clinical trial.

Data Room Features Include:

• Security - Your Ineractive Data Room is hosted in a SAS 70 Level II compliant facility and is encrypted with multiple layers of security and audit controls to comply with 21 CFR Part 11 including:
• Viewing restrictions for selected documents by individual users or groups
• Dynamic watermarking to stamp user name and date/time
• Optional click-through user-definable confidentiality agreements
• User and group security modification functions
• Ease of Use - Site deployment requires minimal training for users and administrators. Designed to reduce extra mouse-clicks and data-entry screens, Trial Interactive allows users to save time and minimize the risk of errors.
  
  
• Convenient Organization - Keep detailed logs sortable by document, user, date, organization, and document rank for simple, convenient tracking of activity.
  
  
• 24/7 Support – Average response times of under three minutes.

For over 16 years, TransPerfect has been a trusted name in business and legal support services for leading financial institutions and every member of the AmLaw 200. We bring that same level of commitment to client service and unparalleled expertise to provide you with cutting-edge online collaboration tools. Our dedicated account managers and technical specialists are available around the clock to meet your every need.

Trial Interactive Clinical Data Rooms reduce study trial start up time and time to final clinical study reports, save on investigative site costs, document archival costs and attract more qualified investigative sites for your global clinical trials.