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Answering Your Challenges,
Today and Tomorrow

We work as your IRT ally, closer than a vendor. When your protocol changes mid-study, we help you adapt fast, protect data quality, and keep the right treatment reaching every participant, on time.

Thirty years building and supporting studies across every design, therapeutic area, and phase.

6,500+trials delivered
500+regulatory approvals supported
3M+participants randomized
100%on-time delivery
100+countries at first participant in
48%+pivotal Phase III
(last 5 yrs)
Solutions

Three Connected Ways to Accelerate Trial Success

Clinical trials are driven by interconnected decisions. By bringing randomization, patient data, and supply strategy together in a single ecosystem, we help sponsors streamline operations, improve collaboration, and run more predictable studies.

IRT

Randomize participants and manage clinical supply on one cloud-native platform: ClinPhone Pro or ClinPhone Pro Core. When the study changes, ClinPhone Pro lets your team update inventory settings, recruitment controls, and operational parameters directly, without waiting on a change request.

Explore IRT

eCOA

Capture high-quality patient, clinician, and site data through a flexible eCOA solution designed for site-based, hybrid, and decentralized trials. Integrated with ClinPhone Pro, it connects workflows, streamlines study execution, and gives participants a consistent experience.

Explore eCOA Solutions

Clinical Supply Management

Access deep expertise in supply forecasting, randomization methodology, and clinical drug planning. Working as an extension of your team, our consultants help you design efficient supply strategies, anticipate operational challenges, and support your study from protocol design through closeout.

Explore Clinical Supply Management
ClinPhone Pro family

Find the Right Fit for Your Study

Every protocol is unique, and few stay unchanged through a trial. Our IRT solutions are designed to fit your study today and adapt efficiently as protocols evolve, amendments arrive, and operational needs change.

Both run on one unified platform and quality framework, with the flexibility, reliability, and scalability to support trials of any size and complexity.

Enterprise / Large Pharma

ClinPhone Pro

Built for enterprise-scale clinical development programs. Configurable to each protocol, adaptable to evolving study requirements, and designed to support global trial portfolios with advanced randomization, supply management, integrations, reporting, and operational oversight.

Explore ClinPhone Pro
Emerging & Mid-Size Pharma / Biotech

ClinPhone Pro Core

Built for biotech and mid-size pharma teams that need a fast path to study launch without compromising quality or future flexibility. Delivered through proven configurations on the same validated platform and quality framework, it gives you speed and reliability today, and room to grow tomorrow.

Explore ClinPhone Pro Core

Start where your study is today. When requirements grow, you build on the same technology foundation rather than replacing it.

Your team

The Experts Who Stay With Your Study

Every study has a dedicated team that stays with your program from design through go-live and study closeout. Project managers, solution designers, data specialists, integration experts, and 24/7 support teams work alongside you, so your IRT adapts as your protocol evolves.

Experience across therapeutic areas, indications, and all phases of clinical development

Expertise in complex designs, protocol amendments, and accelerated study startup

Global delivery teams supporting you across regions and time zones, around the clock

Dedicated specialists in randomization, supply strategy, data management, integrations, and study operations

Company

Who You’re Working With

Behind every study is a team of IRT specialists with experience across therapeutic areas, development phases, study designs, and operational models. From complex adaptive protocols and radiopharmaceutical studies to accelerated startups and global Phase III programs, they design, deploy, and support the IRT each trial needs.

Backed by a global delivery organization, our teams provide strategic guidance, operational expertise, and around-the-clock support through the study lifecycle.

Lucy Neale

VP, Service Delivery

Leads the global delivery organization responsible for study implementation, validation, deployment, and operational support.

[ Head of Solution Design: name to confirm ]

Position

Expertise in randomization methodologies, protocol design, and complex study workflows.

[ Head of Clinical Supply Strategy: name to confirm ]

Position

Specialists in forecasting, drug planning, supply optimization, and operational risk mitigation.

[ Head of Global Support & Operations: name to confirm ]

Position

Delivering 24/7 study support and operational continuity across regions and time zones.

Resources

Insights, Event, and Proof

See where we’ll be next, and how teams like yours put our platform to work.

Get our latest thinking on randomization, supply, and trial data, straight to your inbox.

Let’s Talk About Your Next Study

Tell us where your study is today, and we’ll show you how we can help you move faster with confidence.