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Your Clinical Trial Hub

Mobile. Digital. Informed at the Point of Care.

Clinical Trial Software for Better Outcomes

Fewer protocol deviations. Better trial data quality. Faster, safer, more efficient clinical trials allowing new drugs and treatments to come quickly to market. Our sponsors continue to add more clinical trials on Teckro. In the end, lives are saved, pain and suffering are eased, and quality of life is improved.

Teckro is the digital clinical trial hub for content, communication and collaboration. We connect sponsors, monitors and research site staff with the critical study information they need, when and where they need it - from any digital device.

We take instant answers for granted, especially since the dawn of the smartphone era. For the clinical trial industry – still heavily based on paper and manual processes – answers are anything but immediate. It’s hard work to connect those conducting trials in the field, with the experts who can answer technical, complex medical questions. Immediate answers help everyone involved – sponsor study teams, monitors and clinical research associates (CRAs), investigators and research site staff – to manage faster, safer, more efficient clinical trials.

Here’s how.

Investigators and Research Site Staff

Teckro delivers instant answers at the point of care. Immediate answers empower research site staff to make better-informed decisions; leading to fewer protocol deviations. With current eligibility criteria always on hand from any digital device, more participants are enrolled faster by sites on Teckro. Seeking out paper documents seems unnatural in today’s digitally connected, always-on world. Accessing an online portal via a desktop computer feels equally archaic when most people have a smartphone in their pocket. Teckro cloud-based clinical trial software makes it easy for research site staff to find the answers they need, when they need them - from any device they choose.

When researchers need real-time clarification or guidance, Teckro securely connects sites and study experts with a dedicated channel for support. Auditable and controlled, medical experts can provide instant clarification at the point of care. Teckro consolidates all communication, so sites have one single, simple interface to ask for assistance and to receive timely alerts from study teams.

Biotech and Pharma Companies

Research site staff aren’t the only ones with study questions. Sponsor study teams often wonder whether sites are engaged with their trials and if there is anything they can do to help research staff meet enrollment targets and properly execute protocol instructions. When it comes to participant safety and toxicity management, early visibility is key.

With only periodic reports on site engagement and after-the-fact notices of adverse events, study teams can’t be proactive. Imagine if sponsors could see search activity by site on simple dashboards, including the number of searches and what exactly is being searched. What if early indicators of a potential safety risk could be caught because study teams could see trends in search activities? Going a step further, what if they could proactively initiate outreach to site staff to provide essential guidance for compliance? Teckro cloud-based clinical trial software delivers visibility for sponsors so they know what’s going on with sites and can address potential issues.

Monitors and Clinical Research Associates (CRAs)

Clinical research associates (CRAs) and monitors sit in the heart of a trial. They manage a steady stream of queries from site staff, and responses from sponsors without missing a beat. They also have a critical role to play in the integrity of the trial and its data. Protocol amendments and other timely study information need to be communicated to the right sites at the right time. While technology can ease the burden of their jobs - monitors and CRAs are still working with paper and manual processes. Acting as traffic managers for both research sites and sponsors means connecting the right people with the right answers can be a massive challenge. Teckro cloud-based clinical trial software relieves CRAs and monitors of switchboard duty – meaning they can focus on the higher value activities.

Streamline Communication, Redefine Collaboration

Every clinical trial starts with a question. At Teckro, our question was: “How can clinical trials be more simple, accessible, and transparent?” In today’s digital world, reliable answers are just a tap away. Digital connections allow us to stay engaged with the people in our lives, whether professional or personal. Why shouldn’t the same be true for clinical trials?

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).

Teckro is great! It’s like man discovering fire.

Senior Global Trial Manager, Phase III Oncology Thyroid Cancer

The Champion for Sites

Site success impacts everyone in clinical research. That’s why Teckro is teaming up with SCRS as a Global Impact Partner to better equip those on the ground to run trials simply, quickly and safely.

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