Almac Clinical Technologies are here to help the biopharmaceutical industry bring new therapies to those in need by empowering trial sponsors to proactively manage sites, patients, and clinical supplies through our industry-leading technology and expert consultancy.

The solutions we offer facilitate more than simplifying patient and trial material management - they engineer quality into the clinical trial process.  Our technology provides sponsors and CROs with the visibility and control needed to make data-driven decisions by leveraging advanced supply management functionality coupled with real-time site and patient data in a closed-loop environment.

Almac is uniquely positioned to unlock new efficiency in the clinical supply chain, and to help achieve greater predictability in your projects and programs.

We employ more than 500 professionals dedicated to delivering high-quality solutions and reliable customer service. For nearly two decades, our expertise, energy, and commitment have earned us a reputation as a trusted ally in the drug development process.

Contact us today to see how our technology will surpass your expectations, and experience how our seamless delivery will match your study-specifics regardless of size, phase, or complexity.

 

ART - Accountability and Reconciliation Tracking

Delivering the right solution is an ART™

The accountability and reconciliation process is noted for being time-consuming and error-prone, two characteristics that result in it adding significantly to trial costs and timelines. ARTTM  by Almac is today’s most holistic solution for optimizing the entire accountability and reconciliation process. Find out more

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Disrupting the status quo of eClinical identity management: Removing the burden at clinical trial sites

Disrupting the status quo of eClinical identity management: Removing the burden at clinical trial sites

Drastically reducing the dozens of eClinical software IDs used by busy trial site personnel can greatly benefit and improve any trial. This highly informative webinar discusses the many efficiencies that emerge from implementing a Single Sign-On Interactive Response Technology (IRT). Find out more.

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By the numbers

  • Over 2,000 clinical trials performed with IXRS®
  • Over 2 million patients supported
  • Trials conducted in over 85 countries
  • 65+ Language
  • 10+ Rescue Studies

 

Mega-Trial Experience

  • 510 studies lasting 5+ years
  • 115 studies lasting 4+ years
  • 44 studies with over 500 sites
  • 170 studies with 200 sites
  • 55 studies with more than 5,000 patients
  • 34 trials with 10,000+ patients