Clinical Technologies Areas of Expertise API, Chemical Development & Analytical Services Clinical Services Clinical Technologies Commercial Services Diagnostic Services Pharmaceutical Development Resource Type Search Search Topic Search Select topic Accountability & Reconciliation Tracking Almac ONE Clinical Operations Clinical Trial Research Clinical Trial Supply Clinical Trials Complex Innovative Design Contract Research Organisation Data Integrity Decentralised Clinical Trials Direct to Patient Shipments Drug Supply ECOA IRT IXRS 3 Interactive Response Technology Ixrs Late Phase Monitoring OVERSIGHT Randomisation Regulatory Compliance Study Drug Supply Chain Select Resource type Almac Voice Article Blog Brochure Case study eBook Guide Newsletter Podcast Poster Presentation Publication Q&A Report Technical Publication Technical Sheet Video Webinar Whitepaper What is IRT and How Does it Impact Clinical Trials? Download Brochure Webinar Care is Critical- Lessons Learned from Clinical Trial Inspections Blog Common Randomisation Methodologies Implemented in IRT Webinar How DCT Technology Partnerships a Better Patient Journey, Diversity, and Adherence Webinar Is Your IRT Ready to Support Direct-to-Patient Shipments? Make an Enquiry If you are interested in our Clinical Technologies, then please contact us Contact Us Case study Innovative Electronic Patient Identification System Case study Flexible IXRS® design supports multiple extension studies Case study Ensuring study integrity and reliability during a drug recall Case study Boehringer Ingelheim relies on Almac Clinical Technologies for EDC/IRT integration Case study Accommodating Last-Minute Design Changes Case study Meeting regulatory requirements in Japan: Customised IXRS® manages patient-specific drug orders Case study Weighing the options in addressing a supply issue Case study Total supply chain assurance program turns around global trial Case study Temperature Surveillance Case study Supporting a regulatory submission proactively Case study Supplying costly investigational product: Pre-randomisation approach reduces drug wastage Case study Smooth operations after a cyberattack: Quick thinking and extra coordination preserves drug supply and patient safety Case study Seamless adoption of mid-study protocol change Case study Preparing “Plan B” for a mega study in the event of a supply issue Case study Managing drug and dose assignments Case study Managing 24 protocol amendments across a complex development program Case study Maintaining compliance with new ICH monitoring guidelines Blog Integrating the digital and physical supply chain: Optimal performance, reduced risks, and lower costs Blog Barring the Electronic Door: How to Secure Mobile Devices Used in Clinical Trials Blog Are you equipped with an inspection-ready IRT? Blog 6 Best Practices in IRT Implementation for Clinical Trials in APAC Blog The Burden of Regulatory Compliance Whitepaper Clinical Trials Need Preventative Maintenance Just Like Cars Do, and Here is Why Whitepaper 5 Points of Operational Readiness Report Automated Accountability and Reconciliation Case study Supporting the race for a COVID-19 therapy Blog IRT: A competitive advantage to accelerate clinical trials Report State of the Industry Report: Embracing Trial Change and Elevating IRT Systems Whitepaper The secrets of a successful supply strategy Whitepaper IRT system customisations – necessary or nice to have? Webinar Catching up during COVID: Proven technology for meeting accelerated timelines Case study Accelerating Outcomes with a Pancreatic Cancer Adaptive Platform Video Adaptations and Solutions for Clinical Supply Chain Challenges Article So, you want to run a decentralised clinical trial… Case study How to Add a New Randomized Part to an Ongoing Study in Three Weeks Case study Accommodating a Flexible Visit Schedule Case study Impact of Missing ePRO Data on Clinical Trials Case study Clinical Practice Is Ahead Of Clinical Trials With Technology Use: EMR VS. ePRO Whitepaper A Competitive Race: Accelerating the Development Timeline With A Multi-Trial IRT Programme Whitepaper ART™ – Automated Accountability: Maintaining a chain of custody from release to destruction Meet the Experts Learn more about our experts in your discipline today Find out More
