Asia-Pacific (APAC) IRT Regional Capabilities

Asia-Pacific (APAC) IRT Regional Capabilities

Asia-Pacific (APAC) IRT Regional Capabilities

Asia-Pacific (APAC) IRT Regional Capabilities

 
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Built to Adapt – Most Flexible IRT Platform

For over 20 years Almac Clinical Technologies group has been leading the Interactive Response Technology industry, bringing together the most innovative technology and our unparalleled expertise to empower biopharmaceutical industry and help bring new therapies to patients.

We provide our IRT services in Japan, China, Korea, Singapore, and other APAC locations.

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Almac Clinical Technologies Asia-Pacific (APAC) Experience

45+
Phase I Studies
42+
Phase II Studies
88+
Phase III Studies
10+
Phase IV and Other
92+
Oncology Trials

Supporting 100+ Live Studies!

  • Support 200+ clinical trials
  • Partnership and cooperation with 60+ clients
  • 97% repeat business
  • Familiar and fully compliant with local regulatory requirements
Supporting 100+ Live Studies!

Almac Clinical Technologies IRT Suite

Our solutions are pre-packaged to make IRT platform configuration easy and to save precious time and costs. From a rapid out-of-the-box build to virtually limitless customisations- we tailor our product and services to every study’s needs and requirements.

Almac IRT: Global Reach – Local Support

Recognizing the growth in the number of clinical studies that are now conducted in Asia, Almac Clinical Technologies has been expanding our physical presence in the region for years.

30+ project management and technical support professionals

  • Direct language support: English, Japanese and Chinese
  • 9 AM – 6 PM China/Singapore local time
  • Other time zones supported by our UK and US teams with interpreters
  • Contact via phone, email, and live chat
  • Adhere to Almac global SOPs

IXRS®3 IRT System in China

120+
Studies
30+
Local Sponsors
10+
Years Experience
100%
Repeat Business

 

IRT studies Tokyo China Singapore

We’ve been successfully expanding our footprint in China for over 10 years, becoming the leading IRT solution on the market

  • Direct language support
  • Local business hours
  • Familiar and fully complied with local regulatory requirements – HGRAC
  • Highly involved with local industry events – China IRT Forum, DIA China and ChinaTrials.

Our teams of IRT experts guide you through the process with ease and transparency and take preemptive steps to keep the study inspection-ready and in compliance 24/7 – so you can confidently cross IRT off your list.

Contact us today

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.

Contact us
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