Teckro is the hub for digitally connected trials. Study stakeholders are connected with the content, communication and insights they need to perform their role, enhancing study execution and enabling greater focus on patient safety and data integrity.

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, static study documents are transformed into a critical data source for engagement and trial conduct. Study instructions and essential guidance are always available, especially at the point of care.

With answers within reach from any digital device or smartphone, 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.”

Teckro 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, changing how 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 supports multimedia study content, allowing study teams to share information in varied formats for increased site accessibility and engagement. Critical resources are digitally available to research staff in a way that is more efficient, more powerful, and more easily consumed for greater study outcomes. Sites can access the digitized protocol and other study documents, alongside videos for complex clinical procedures or study relevant podcasts, directly from the mobile app.

Every interaction with the protocol now becomes a data point, providing valuable insight into site engagement and activity trends. Study teams gain real-time visibility, enabling identification of potential safety issues or the need to clarify instructions in the protocol. CRAs can identify underperforming sites and triage accordingly; focusing their efforts to help ensure study goals are met.

Real-time Guidance

Even with study content in their pocket, investigators and research staff may still have questions. Until now, those questions could take hours, days or longer to be answered, 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 with 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. Links can be embedded in messages, taking sites directly to associated resources. Teckro cloud-based clinical trial software enables proactive compliance, with messages delivered to the right people at the right time. 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 globally by more than 34,000 research sites 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, inflammation, nephrology, neurology, virology, and urology. We also have rare disease clinical trials.  

Unlike traditional clinical trial software, Teckro cloud-based clinical trial software is quick to set up and even faster to deploy. It’s accessible from a mobile application or through a secure website. Study user set up on the Teckro platform is managed seamlessly by our team, collaborating with sponsors to accurately assign permissions and site allocation. The protocol is digitized and made available to the right users at the right time with prompt release of amendments. Once study documents are on Teckro, version control management is fast and simple for study teams and monitors. Immediately upon release of an approved amendment, they can process document version assignments as appropriate per site, directly from the app.  

Teckro is compliant with industry regulations, including FDA's 21 CFR Part 11.