Solving the biggest clinical trial challenges for sites, sponsors, and participants.
Request a demo
Solving the biggest clinical trial challenges for sites, sponsors, and participants.
Request a demo
Solving the biggest clinical trial challenges for sites, sponsors, and participants.
Request a demo
Solving the biggest clinical trial challenges for sites, sponsors, and participants.
Request a demo
Almac eCOA
Electronic Clinical Outcome Assessments for Global Trials
Flexible. Accurate. Patient-Focused.
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Almac Trial Coordinator™
Fully interoperable eClinical solutions suite
Uniting trial workflows. Guiding study teams. Retaining participants
Almac Trial Coordinator™ is a fully integrated eClinical platform designed to simplify and unify clinical trial operations. By combining IRT, eCOA, eConsent, and Visit Management into one intuitive interface, it tackles today’s biggest challenges: system fragmentation, data complexity, compliance risk, integration barriers, and site and participant burden. Choose from flexible, ready-to-deploy modules, or opt for full integration within Almac’s unified ecosystem to streamline your trials and accelerate success.
Almac Trial Coordinator™ Key Features
Discover how Almac Trial Coordinator™ transforms clinical trials
IRT, EDC, eCOA, eConsent,
Visit Management
Workflow Management
including 3rd party systems
Real-Time Dashboards
for sponsor oversight
Role-based workflows
for site enablement
Rapid setup
and protocol amendments
24/7
Multilingual support
IXRS®3 IRT Solution
The most flexible Interactive Response Technology
platform in the industry.
For over 25 years Almac Clinical Technologies has been leading the IRT industry, bringing together the most innovative technoloy and our unparalleled expertise to empower the biopharmaceutical industry and help bring new therapies to participants.
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eCOA
Flexible, accurate and participant focused electronic assessment capture built for global trials.
Almac’s eCOA solution delivers flexible, accurate, and participant-focused electronic assessment capture. Fully flexible on it’s own or as part of the Almac Trial Coordinator™ ecosystem, it simplifies data collection, enhances compliance, and reduces burden for participants and sites.
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eClinical Solutions for Clinical Trials
Empower your clinical trials with cutting-edge eClinical solutions designed to streamline every step of the process. From secure and compliant eConsent to centralized data management through Almac One, and efficient visit management tools, our integrated platform ensures accuracy, transparency, and speed. Simplify complexity, enhance participant engagement, and drive smarter decisions with solutions built for modern clinical research.
eConsent
Almac’s eConsent platform is designed to streamline both electronic and paper-based consent processes.
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Almac ONE
A unified clinical trial supply solution that manages participant recruitment, clinical supplies, and IRT, creating a responsive and data-driven supply chain.
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Visit Management
Empowers sponsors and site to deliver efficient, compliant, and participant-friendly visit scheduling.
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Our Services and Expertise
Our team combines deep scientific knowledge with innovative strategies to deliver comprehensive support for your clinical trials. From expert biostatistics and consulting to advanced adaptive trial designs, we help optimize study efficiency and outcomes. Through seamless integrations and strategic partnerships, we ensure your trials are connected, compliant, and positioned for success. Trust our expertise to navigate complexity and accelerate your path to breakthrough results.
Biostatistical and Consulting
Complex innovative trial design randomisation techniques and IRT implementation.
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Adaptive Trial Designs
Focused expertise to implement complex innovative study designs.
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Integrations and Partnerships
Product integrations and partner network with no exclusions.
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Our Global Reach
Delivering excellence worldwide
At Almac Clinical Technologies, we proudly support clinical trials across the globe through our strategically located facilities in EMEA, US and APAC. This extensive footprint ensures seamless delivery, local expertise, and 24/7 support for sponsors and sites – wherever your study takes place.
