Teckro vs RealTime

Teckro transforms your clinical trial protocol into a hub of communication and collaboration. It’s a digital platform that connects all study stakeholders with the knowledge they need, when they need it. Drugs from trials powered by Teckro have been granted priority review and approval by regulators in the US and Europe. Thousands of investigators and 20,000+ sites around the world rely on Teckro to execute clinical trials from biopharma sponsors, including 12 out of the Top 20 pharma companies. We support all therapeutic areas, all phases, and any trial model, whether traditional, virtual, or a hybrid approach - if Teckro isn't used on your clinical trial, ask your study manager for it.

Our latest version includes all major function of CTMS, eDOCS and eSOURCE. - CTMS features include a complete calendar for scheduling and viewing the users "My Calendar". View full subject profiles, study enrollments, complete visits, view study contacts and much more! Easily display inclusion and exclusion criteria for a particular study while also having the ability to "Refer a Patient". Patient referrals drop directly into your RealTime-CTMS Study Recruitment Roster and site staff are alerted to the new study lead. - eDOCS includes eSignatures utilizing fingerprint or face ID technology. View all regulatory documents for user-assigned studies, access the current versions of the Protocol, ICFs, or any other important study document while on the go. - eSOURCE includes the full suite of eSOURCE services that are available on the desktop version of RealTime-eSOURCE. Collect visit data on your phone or tablet, voice dictate notes or impressions, eSign lab documents with a Part-11 compliant PIN and much more! - Other features include a Contacts Section that allows users to view Personal Contacts, Study Sponsor/CRO Contacts and Research Staff Contacts.