Digitizing Multilingual COAs: A Practical Guide
Download our guide to ensuring seamless digitization of your multilingual COAs. ...
Harnessing AI in Pharmacovigilance: Insights from World Drug Safety Amsterdam 2024
Pharmacovigilance professionals face an escalating challenge: data overload. From AI-powered transcription and case triage to automated literature translation, insights from the World Drug Safety Congress 2024 showcased practical solutions for streamlining workflows and reducing costs. Download the PowerPoint from Christine Buggle's presentation on this topic....
LifeSci Talks COA Series | AI-Powered Innovations in Clinical Trials: Optimizing Every Step
Explore how artificial intelligence is rapidly changing the landscape of clinical trials, from discovering new therapies and complex calculations to protocol optimization. Discover how AI can generate study protocols, consent forms, and more, saving time and resources. Join us to unravel the potential of AI in reshaping the future of medical research and clinical trial operations....
The Ultimate Clinical Trial Translations Checklist
Clinical product development is an elaborate endeavor executed through a complex web of processes that are in large part accomplished through various document and communication work streams. These work streams can represent a significant source of cost, risk, and time. When a study operates across cultures, countries, and continents, these pain points of cost, risk, and time are compounded by the addition of translation and localization requirements. Study teams who can...
C3 Summit 2024 - London
Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to commercialization. The event offers sponsors, CROs, and biotech professionals opportunities to share knowledge, gain industry insights, and network. Please fill out the form to access the session...
C3 Summit 2024 - Princeton
Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to commercialization. The event offers sponsors, CROs, and biotech professionals opportunities to share knowledge, gain industry insights, and network. Please fill out the form to access the session...
The Ultimate Guide to AI in Pharmacovigilance and Safety Reporting
Pharmaceutical companies face stringent compliance requirements and tight deadlines for reporting safety cases throughout clinical research and development. To protect patient safety and avoid penalties from regulatory authorities, pharmacovigilance teams must submit in-language reports on time. AI technology offers transformative solutions to these challenges and opens the door for increased efficiencies throughout event observation, detection, and monitoring. This guide...
Translation and Cultural Adaptation of Clinical Outcome Assessments (COAs): Is Machine Translation a Viable Option?
As technology continues to advance and the need to expedite drug development increases, the applications of Machine Translation (MT) and Artificial Intelligence (AI) in the translation process should be further explored. The capabilities of iterative learning and feedback can serve as a tool for translation, but the limitations should be considered. This poster will compare human translation (HT) and machine translation (MT) in the back translation step for Clinical Outcome...
Transforming Pharmacovigilance with AI and Automation
Explore how AI enhances safety reporting, automates processes, and drives compliance in pharmacovigilance....
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Trial Interactive Customer Summit, OpTImize
Join us for the OpTImize Summit, Trial Interactive’s exclusive annual customer event. This invitation-only conference features networking opportunities, product showcases, inspiring client success stories, and thought-provoking sessions led by Trial Interactive experts and industry guest speakers. ...
C3 Summit London 2025
Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to commercialization. The event offers sponsors, CROs, and biotech professionals opportunities to share knowledge, gain industry insights, and network. ...
Top 10 Prompts to Ask ChatGPT for Optimizing Clinical Trial Recruitment Strategies
Patient recruitment and engagement are critical to the success of clinical trials. Yet despite the tremendous progress made in drug development, recruitment and retention remain major challenges. Over the last 25 years, the industry has attempted to crack the code; however, 86% of trials still don’t meet original enrollment goals. A bit curious yet somewhat cynical, I turned to ChatGPT to see if it could shed some light on this age-old problem. If you’re like me and...
Clinical Evidence in Digital Health: Considerations for Multi-Country Evidence Generation
The global adoption of digital health solutions has revolutionized healthcare delivery, offering unprecedented opportunities for innovation in patient care, diagnostics, and disease management. However, the generation of robust clinical evidence to support these technologies across diverse regulatory, cultural, and healthcare system contexts remains a significant challenge. In this webinar, Alexandra Crane, VP of COA, Digital Health, and Regulatory Solutions at TransPerfect...
Top 10 Prompts to Ask ChatGPT for Optimizing Clinical Trial Recruitment Strategies
Clinical trial recruitment is a complex process that requires strategic planning and data-driven decision-making. Use these AI-powered prompts to refine your approach and enhance participant engagement....
The Future of Patient Recruitment: AI Trends and Technologies for 2025
As artificial intelligence continues to change the way pharma companies engage with patients globally, a critical question emerges: how do we ensure patients remain at the heart of clinical research? In this webinar with Innovative Trials, SOGLIA, Subjectwell, and Pleco Therapeutics, you’ll learn about the current landscape and future outlook of shaping patient-centric AI to enhance global recruitment efforts. Join us to hear from industry experts as they share real-world...
Faster Submissions, Smarter Workflows: Lessons from Sanofi's AI-Powered Translation Strategy
In this session, learn how Sanofi has transformed its translation processes using centralized management by expert project managers, automated workflows, and integration of TransPerfect’s GlobalLink platform with Veeva eTMF. You’ll gain insights into Sanofi’s pragmatic, phased approach, including leveraging automation and AI-powered workflows. The result is a dynamic digital ecosystem that captures feedback, drives continuous improvement, and achieves over 30% savings in time...
Meeting the MDR & IVDR Content Challenge: New AI and Automation Solutions for New Requirements
The European Union's introduction of the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) marks a significant shift towards enhanced transparency in the medical device sector. While these regulations are designed to strengthen patient safety following several high-profile device failures, they have also created complex labeling updates and post market reporting requirements. Medical device companies must now navigate these complexities...
The Future of Patient Recruitment: AI Trends and Technologies for 2025
As artificial intelligence continues to change the way pharma companies engage with patients globally, a critical question emerges: how do we ensure patients remain at the heart of clinical research?In our upcoming webinar with Innovative Trials, SOGLIA, SubjectWell, and Pleco Therapeutics, you’ll learn about the current landscape and future outlook of shaping patient-centric AI to enhance global recruitment efforts. Join us to hear from industry experts as they share real...
The Journey to TMF Rescue: A Case Study in Quality and Compliance
Step into the world of Trial Master File management with this engaging and informative session, The Journey to TMF Rescue: A Case Study in Quality and Compliance. This webinar unpacks how critical TMF deficiencies were identified and successfully resolved through a methodical and practical approach.Join us as we explore the process of conducting a comprehensive gap analysis, implementing effective remediation strategies, and applying robust quality control measures to achieve...
LifeSci Talks COA Series | Data Without Interpretation is Meaningless: Unlocking Inherent Value Within the Numbers
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Elizabeth (Nicki) Bush, Executive Director and Global Head of Endpoint Strategy and COA Measurement at OPEN Health Group to discuss the growing complexity of collecting and interpreting patient data. With insights from the recent FDA workshop around Patient-Focused Drug Development (PFFD), the two discuss the importance of integrating measurement science early in...