www.triall.io Open in urlscan Pro
63.35.51.142  Public Scan

Form analysis
0 forms found in the DOM

Text Content

This website stores cookies on your computer. These cookies are used to collect
information about how you interact with our website and allow us to remember
you. We use this information in order to improve and customize your browsing
experience and for analytics and metrics about our visitors both on this website
and other media. To find out more about the cookies we use, see our Privacy
Policy

If you decline, your information won’t be tracked when you visit this website. A
single cookie will be used in your browser to remember your preference not to be
tracked.

Cookies settings
AcceptDecline

 * Menu
   
   eClinical Solutions
    * EDC
    * eSource
    * ePRO / eCOA
    * eConsent
    * Virtual Visit
    * RTSM
    * 
   
    * CTMS
    * eTMF
    * Wearable Integration
    * Medical Coder
    * Clinical Adjudication
    * 
   
   ECLINICAL SOLUTIONS
   
   View all
   Services
    * Patient Recruitment
    * Data Management
      
    * Regulatory Affairs
    * Quality Management
    * Clinical Trial Management
    * Clinical Trial Design
    * 
   
   SERVICES
   
   View all
   Cix
    * The Clinical Insights Exchange (CIX) represents Triall's future product
      vision. It is a federated marketplace to promote privacy-friendly reuse of
      clinical trial data. Click the button below to learn more.
    * 
    * 
    * 
   
   CIX
   
   Learn more
   Resources
    * Decentralised Clinical Trials
      
    * Computerised Systems
    * Complex Clinical Trials
   
   More
    * Articles & News
      
    * About TRL

Get in touch



STREAMLINE YOUR CLINICAL TRIALS WITH TRUSTED ECLINICAL SOFTWARE & SERVICES

Triall offers the technology, tools, and expertise to drive your clinical
development forward. We empower clinical research professionals throughout the
full clinical trial lifecycle—from study design, to execution, and post-study
activities.


Learn more




In Collaboration With

Our software and services


WE COMBINE ADVANCED TECHNOLOGIES WITH OPERATIONAL EXCELLENCE


ECLINICAL SOLUTIONS

Our interoperable suite of eClinical solutions can be configured to your unique
study needs, offering advanced web-based, mobile, and wearable capabilities
for decentralised, hybrid, and centralised clinical trials.
Learn more




RESEARCH SERVICES

Triall has built a network of selected CRO partners that each excel in their
respective domains, allowing us to offer you a truly end-to-end service offering
that covers all key aspects of clinical trial design and execution.
Learn more




CLINICAL INSIGHTS EXCHANGE

Triall’s Clinical Insights Exchange (CIX) unlocks informed data-driven insights
for study planning and design by applying privacy-enhancing technologies to
analyse a database of historical clinical trial data.
Learn more




... TO HELP YOU NAVIGATE THE COMPLEXITIES OF CLINICAL RESEARCH WITH A TRULY
CONSOLIDATED OFFERING


TECHNOLOGY


Purpose-built eClinical solutions

Decentralised technologies

Privacy-enhancing techniques

Artificial intelligence


TOOLS


Data-driven insights

Risk mitigation

Quality control

Inspection readiness


EXPERTISE


Strategic vision

Specialist knowledge & expertise

Quality & compliance

Scientific excellence
eClinical Infrastructure


OUR ECLINICAL SOLUTIONS LEVERAGE AN INDUSTRY-VALIDATED TOOLKIT

Our eClinical solutions run on top of TrialKit, a clinical trial software
toolkit developed by Crucial Data Solutions. Since 2010, TrialKit has been
validated by over 8,000 studies across the globe.

8,000
+
Studies

Lorem ipsum dolor sit amet, consectet adipiscing elit arcu.

1,000
+
Sponsors & CROs

Lorem ipsum dolor sit amet, consectet adipiscing elit arcu.

10,000
+
Users

Lorem ipsum dolor sit amet, consectet adipiscing elit arcu.

All
Continents

Lorem ipsum dolor sit amet, consectet adipiscing elit arcu.

Testimonials


OTHERS ABOUT OUR ECLINICAL SUITE

TrialKit is appreciated for its intuitiveness, versatility, and flexibility by
clinical research professionals across the board.

“A fantastic EDC. Our clients love it and we do too! (...) It is clear, concise,
and very easy to navigate.”
‍

Data Manager
CRO, 11-50 employees

"I have used many other systems. [This] is by far my favorite. The Customer
Support is better than anything I've seen (...) I love this product and support
staff."

Clinical Data Manager
Pharmaceuticals, 501-1000 employees

"I was able to turn around an entire study's EDC set-up within 3 weeks of
getting contracts signed."
‍

Director, Clinical Program Management
Pharmaceuticals, 11-50 employees

"Unlike all other EDCs in the market. My experience with this tool stands out. I
must say it is highly convenient for any user in any specific role.”

Sr. Clinical Data Manager
Pharmaceuticals, 51-200 employees

"Infinitely customizable eCRF requiring no coding knowledge. I’m extremely
satisfied and don’t understand why anyone would use any of the extremely
expensive alternatives.”
‍

Clinical Project Manager
Medical Devices Consultancy, 1-10 employees

"Our business needed a cost-effective, easy-to-use solution that could support
data capture for a complex, large-scale, global, medical device registry. (...)
Overall, our experience has been very positive, and we would consider this
platform for future studies without hesitation.”

Sr. Director Clinical Affairs
Medical Devices, 51-200 employees

  Previous
Next  



WANT TO LEARN MORE?

Our product specialists are available to answer all of your questions. Reach out
to us to talk or to schedule a live product demo today.

Schedule a demo
Articles & News


FOLLOW OUR LATEST INSIGHTS ON CLINICAL TRIAL TRENDS AND TECHNOLOGIES

We regularly publish articles and videos about industry trends, changing
regulations, and emerging technologies in clinical trials.

View all



DATA-INFORMED PROTOCOLS: THE NEXT FRONTIER IN CLINICAL TRIAL DESIGN & CONDUCT

In this article, we dive into the key benefits and implementation drivers of
data-informed protocol development in clinical research.


Deep Dives

15
 min read


BEYOND RANDOMISED CONTROLLED TRIALS: HOW EXTERNAL CONTROL ARMS COULD CHANGE THE
GAME

In this article, we unpack the promise of external control arms, covering
benefits, design considerations, challenges, and success stories.


Deep Dives

20
 min read


DIGITALISING CLINICAL TRIALS: A CRO PERSPECTIVE ON DIGITAL TRANSFORMATION

Interview with Nick van den Bulk, Head of Clinical Operations at CR2O, to talk
about the company’s digital transformation journey.


Ecosystem

10
 min read


SUBSCRIBE TO OUR LATEST INSIGHTS

Sign up to receive our articles on industry trends, changing regulations, and
emerging technologies in clinical trials.

Subscribe







CLINICAL TRIAL SOFTWARE

 * Product Overview
 * EDC
 * eSource
 * ePRO / eCOA
 * eConsent
 * Virtual Visit
 * Wearable Integration
 * Medical Coder
 * Clinical Adjudication


 * CIX
 * CTMS
 * RTSM
 * eTMF
 * Reporting & Analytics
 * Payments Manager
 * AI (EHR to EDC)
 * Blockchain Proof


RESEARCH SERVICES

 * Service Overview
 * Patient Recruitment
 * Data Management
 * Biostatistics
 * Pharmacovigilance
 * Quality Management
 * Auditing
 * Clinical Trial Design
 * Clinical Trial Management
 * Consortium Management
 * Insourcing
 * Medical Writing
 * Regulatory Affairs


MORE

 * Resources
 * Articles & News
 * About Us
 * About TRL
 * FAQ
 * Contact
 * Subscribe


Privacy Policy

Cookie Policy

Disclaimer
© 2023 Triall (Clinblocks B.V.) - All rights reserved.