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YOUR CLINICAL TRIAL HUB

Mobile. Digital. Informed at the Point of Care.

Get a demo





CLINICAL TRIAL SOFTWARE FOR BETTER OUTCOMES

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.


EXPAND FOR MORE DETAILS ON WHO BENEFITS FROM TECKRO

Teckro is the digital clinical trial hub for content, communication and
insights. We connect sponsors, monitors and research site staff with the
critical study information and guidance 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 information they need and the experts
who can answer technical, complex medical questions.

The Teckro solution:


INVESTIGATORS AND RESEARCH SITE STAFF

Teckro delivers instant answers at the point of care, empowering research site
staff to make better-informed decisions and improving outcomes. Seeking out
paper documents is unnatural in today’s digitally connected world. Accessing an
online portal via a desktop computer is 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 answers. With current eligibility criteria
immediately on hand, sites on Teckro are equipped to make the best decisions
quickly about patient enrollment. Alerts from their study team with timely
guidance about an upcoming visit mean site staff are prepared for the best
patient experience.

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

Yet, 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 easily
view activity per site, including trending search terms and message open rates.
What if early indicators of a potential safety risk could be caught because
study teams could see trends in site activity? 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 and improve engagement.


MONITORS AND CLINICAL RESEARCH ASSOCIATES (CRAS)

CRAs and monitors sit at the heart of a trial. They manage a steady stream of
queries from site staff and responses from sponsors. They also play a critical
role in the integrity of the trial and its data. Protocol amendments and other
study information need to be communicated to the right sites at the right time,
which is a challenge with paper documents and manual processes. 

Teckro cloud-based clinical trial software unblocks essential monitor activity
by enabling agility and efficiency and reducing the time taken to complete
auxiliary tasks. Teckro centralizes content and communication, negating
navigation of numerous portals and passwords and the need to sift through
scattered texts, emails and voicemails.

With approved study documents always in the hands of research staff and a direct
communication channel available between sites and study experts, Teckro
cloud-based clinical trial software relieves CRAs and monitors of switchboard
duty. As site self-sufficiency increases, monitors can focus on fulfilling vital
trial monitoring and reporting obligations. As a mobile app, Teckro provides
real-time study oversight on-the-go, enabling productivity during travel. The
simple interface also allows easy site and user management and document version
assignment.  




TECKRO IS GREAT! IT’S LIKE MAN DISCOVERING FIRE.

Senior Global Trial Manager


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. The same should be true for clinical trials.


EXPAND FOR MORE DETAILS ON HOW TECKRO WORKS

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.  




CONSIDERATIONS FOR LGBTQ+ INCLUSION IN CLINICAL RESEARCH

Inclusion starts with listening. We partnered with the Center for the
Information and Study of Clinical Research Participation (CISCRP) to amplify the
voice of the LGBTQ+ community. Read more about engaging LGBTQ+ patients.

View the report



5 WAYS TO MAKE YOUR CLINICAL TRIAL WORK AT LIGHTSPEED

When clinical trial operations move quickly, investigators and research staff
focus more on patient care. Stakeholders become interconnected and sponsors gain
new levels of insights into trial performance. Explore the five ways to increase
speed and efficiency.

Get the paper

Learn more


LISTEN: TECKRO TALKS WITH EXPERTS



Our fresh-thinking, ad-free podcast Totally Clinical: Trial Triumphs & Rad
Trends explores engaging topics among diverse stakeholders in the clinical trial
ecosystem.






THE UNIQUE CHALLENGES OF PHASE I ONCOLOGY TRIALS

Genentech’s Dan Otap, and industry expert Jenn Weinberg, talk about overcoming
the challenges of Phase I oncology trials.




HOW HIGH CRA TURNOVER AFFECTS SITE RELATIONSHIPS

Remote Site Monitor Ashley Margo and Teckro’s Maria Milas discuss how CRA
burnout can impact the relationship between sponsors and sites.




LEVERAGING VIDEO FOR CLINICAL TRIAL SUCCESS

David Grew, radiation oncologist and founder of video platform PRIMR, explains
how he transformed his paper sketches into video for trial patients.




AN INSIDER VIEW ON CLINICAL TRIALS IN UKRAINE

Roman Fishchuk, Teckro user, physician and principal investigator, describes the
pressures of life in wartime Ukraine and implications for clinical trials.




BREAKING DOWN BARRIERS FOR BETTER LGBTQ+ HEALTH

Stewart O’Callaghan, founder and CEO of Live Through This, the UK’s only LGBTQ+
cancer charity, explains breaking down barriers for better LGBTQ+ health.




WHAT IF BIOPHARMA THOUGHT “COLLABORATE FIRST”?

Virginia Nido from Roche shares her vision for greater pre-competitive
collaboration.




MORE PERSPECTIVES ON CLINICAL TRIALS

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How to improve cancer clinical trial efficiency and safety.

CUSTOMER STORIES


ALIGNING WITH STUDY SITES FOR ENROLLMENT SUCCESS

A Top 10 sponsor uses Teckro to support study sites for fast, accurate
enrollment decisions.

VIDEOS


MISSION DRIVEN: OUR STORY ON MAKING AN IMPACT

Discover why Teckro was founded to simplify and modernize clinical trials.

BLOG


ONE TREE PLANTED: A PARTNERSHIP TAKING ROOT

CEO Gary Hughes introduces Teckro's new partnership with non-profit One Tree
Planted.

BLOGDEI


HOW TECKRO ADVANCES SUSTAINABILITY, DEI AND SMARTER CLINICAL TRIALS

Jeanne Hecht examines Teckro's role in environmental, social and governance
goals.

BLOGSPONSORRESEARCH SITE


WHY EVERYONE WINS WITH PAPERLESS CLINICAL TRIALS

Malia Lewin examines sustainability trends, patient outcomes and reduced costs.

BLOGRESEARCH SITE


HOW TECKRO IS REVOLUTIONIZING MY DAY JOB

Grayson Scott from Centricity Research, describes how Teckro supports daily
duties.

PODCASTRESEARCH SITE


HOW TECKRO IMPACTS THIS RESEARCH SITE SUPERVISOR’S DAY JOB

Grayson Scott from Centricity Research discusses his positive Teckro user
experience.

PODCASTRESEARCH SITE


AN INSIDER VIEW ON CLINICAL TRIALS IN UKRAINE

Teckro user Dr. Roman Fishchuk discusses the state of clinical trials in
Ukraine.


EVERY CLINICAL TRIAL STARTS WITH A QUESTION




THE ANSWER

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