Teckro cloud-based clinical trial software connects investigators and research site staff, sponsors and monitors with both each other, and the critical study information they need, when they need it. The digital hub of content, communication and collaboration, Teckro transforms clinical trial protocols from a static document into a critical data source for engagement and trial conduct.
It’s time to finally retire paper protocols and cut the cord with fixed desktop computers that are inconveniently out of reach for research staff and investigators. With Teckro cloud-based clinical trial software, study instructions and essential guidance are always available on demand – any time, any place.
With answers within reach from any digital device – it’s faster, easier and simpler for investigators and site staff to enroll the right participants and protect patient safety. Teckro is the 21st Century version of a “quick reference guide” – accessible from any smartphone or digital device.
Teckro cloud-based clinical trial software gives sponsors and monitors a new level of visibility and engagement with research sites. Study teams, monitors, investigators and research site staff can all stay aligned with Teckro clinical trial software.
As the hub for communication and collaboration, Teckro changes how study stakeholders work together. No more disparate, siloed communications across channels like email and text message. Communication in Teckro is auditable and exportable for inclusion in the TMF and ISF, eliminating extra steps to log interactions.
The main features of Teckro include:
On-Demand Protocol
Teckro cloud-based clinical trial software puts the protocol and other study documents (such as lab manual, investigator’s brochure, etc.) in the hands of sites – so critical information is available anywhere, anytime. Research staff and investigators can find study answers from their pocket, day or night.
Every interaction with the protocol now becomes a data point, providing valuable insights into site engagement and search trends. From the Teckro dashboard, study teams have real-time visibility into search terms, enabling identification of potential safety issues or the need to clarify instructions in the protocol. CRAs can identify underperforming sites, and focus their efforts to help them meet study goals.
Real-time Guidance
Even with the protocol in their pocket, investigators and research staff may still have questions. Until now, those questions could take hours or days – maybe longer – to get an answer after being routed to the right person. With Teckro cloud-based clinical trial software, investigators and research site staff have an instant, compliant, auditable channel to initiate a query to a dedicated group of study experts, directly from their smartphone. This means no question goes unanswered and site queries are resolved quickly.
Proactive Outreach
Forget generic, broad newsletters. Think of Teckro as the “virtual coach” on the shoulder of research staff. Study teams can send specific messages to prepare sites for an upcoming patient visit, share tips for study enrollment, or alert them of critical updates. Teckro cloud-based clinical trial software enables proactive compliance with messages delivered to the right people at the right time. Through the Teckro dashboard, study teams have visibility into what messages are being sent to whom and when, and they can track communication effectiveness with open rates.
Quick Site Feedback
Teckro also gives sponsors and monitors a simple way to measure site sentiment. This could be to identify challenges with enrollment or to gather feedback on the trial design. Feedback is easily captured with Teckro through a simple web-based survey tool.
Teckro is Global
Today, Teckro cloud-based clinical trial software is used by more than 23,000 research sites globally for a wide variety of disease areas. Teckro is used during all phases of clinical trials. We support trials for oncology, central nervous system, infectious disease, cardiovascular, metabolic disorders, gastrointestinal, immunology, respiratory, dermatology, and musculoskeletal disorders. We also have rare disease clinical trials.
We can move as quickly as our sponsors need to get studies live. The urgency of COVID-19 trials accelerated timetables, with speed never before seen from the pharmaceutical industry. Teckro partnered with our sponsors to make sure we were ready to go with these crucial and time sensitive clinical trials. One of our sponsors completed enrollment for their COVID-19 trial a full three months ahead of schedule.
Unlike traditional clinical trial software, Teckro cloud-based clinical trial software is rapidly available. It’s accessible from a mobile application or through a secure website. Study users are added with the right permissions based on their roles, and associated to the correct site(s). Clinical trial documents are digitized and added to the Teckro platform, so they are immediately searchable. Teckro also takes the stress out of version control so that any updates or protocol amendments are released to the right sites at the right time.
Teckro is compliant with industry regulations, including the FDA 21 CFR Part 11. Communication is audit-ready and can be exported for trial reporting, including the trial master file (TMF) and investigator site file (ISF).
