IntraLinks® On-Demand Workspaces™ can help you accelerate Phase I to Phase IV clinical trials by connecting study participants in a secure environment—so you communicate, collaborate and disseminate information at record speed. From study start-up to study closure, IntraLinks helps you streamline critical processes and reach crucial milestones faster, while helping you comply with 21 CFR Part 11 and other regulatory guidelines.

Simplify Site Contracting
Get your contract and budget negotiations done more quickly by exchanging drafts and other key documents securely online. No matter how many sites you have, IntraLinks helps you get them on board quickly and effortlessly.

Shorten Study Start-up Time
Distribute and collect all of your investigator packets and regulatory documents online—so investigators and IRBs don’t have to wait for mail to arrive. IntraLinks automatically tracks receipt of critical information, and you can even receive electronically signed copies in return.

Manage Trial Information More Efficiently
Exchange information among trial participants throughout the study. Create a single, secure repository for monitoring reports, data clarification forms, lab information, summary reports, patient diary data and adverse event reports. Manage and track site status by keeping tabs on the completion of key documents and tasks.

Enhance Study Conduct and Improve Your Response
Amending protocols and sending safety notifications are crucial processes that must be handled without errors or delays; they can also be quite costly, especially in larger studies. With IntraLinks, you can distribute these documents instantly to IRBs, investigators, regulatory groups and safety departments. And because everything is tracked electronically, you’ll always know who has accessed the latest version, and when.

Sign Documents with SAFE e-Signatures
With IntraLinks, investigator site personnel can access and sign documents electronically using SAFE standards. Sponsors can reduce cycle time by distributing documents online and receiving signed PDFs back directly through their IntraLinks workspaces. Investigator site personnel can reduce the need for paper, and spend less time sorting through mail or trying to locate key documents.