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LifeSci Talks COA Series | Decoding Decentralized Trials: Navigating Novel Decentralized Research Challenges and Complexity

DCTs have picked up significantly in previous years, catalyzed by the pandemic and a move to remote research. With this move comes a host of new challenges, including those surrounding technical interoperability, resistance to adopting new technologies, and the need for flexibility in technology uptake at research sites. With additional considerations to be made, such as ensuring regulatory compliance, and enforcing standardized metrics in assessing DCT performance, this...

Data Annotation for Life Sciences

At DataForce, we specialize in elevating real-world clinical data through precise and efficient annotation services. From real-time adverse event (AE) detection for pharmacovigilance to social listening for trend identification, our expertly annotated datasets empower AI models, fostering innovation and success in clinical research and development.....

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COA White Paper | The Tale of Two Trials

In “The Tale of Two Trials,” Mark Wade takes an in-depth look at the benefits and drawbacks of the traditional, paper-based outcomes assessment method, as well as the advantages of the emerging electronic clinical outcomes assessment (eCOA) solutions. With each having the potential to affect data quality, timelines, and overall trial cost, the choice between them is a much discussed topic....

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LifeSci Talks COA Series | Licensing Challenges vs. eCOA Vendor Capabilities

In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Stacey Higgins, Associate Director, COA & Digital Implementation, to cover the intricacies of clinical trial licensing, contract variations among eCOA providers, the importance of sponsor involvement, and the challenges of validated translations. Explore the complexities that can arise in these critical aspects of clinical trials...

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Clinical Content Trends: 2023 Reflections and 2024 Projections

Over the past decade, the pharmaceutical industry has transformed significantly, giving way to breakthrough therapeutics and innovations for improved patient outcomes around the world. With these changes, there’s also been significant developments in the way organizations are approaching business, and with it, the processes that surround managing clinical content. In this webinar, our experts will reflect on some of the most significant insights that 2023 has regarding...

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Achieving Global Success in Clinical Trial Recruitment

TransPerfect's GlobalLink Connect integration with Adobe Experience Cloud enabled one of the world’s largest pharmaceutical companies to help visitors in 17 countries and 13 languages identify clinical trials that might be right for them or their loved ones....

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PRO Scheduling Considerations: Assessing Patient & Caregiver Burden in Clinical Trials

In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with Andrew Lloyd, Director at Acaster-Lloyd Consulting, to spotlight the burden of clinical research for patients, and their caregiver/family dynamics. From ethical considerations surrounding patient/caregiver consent, to the intricate timing challenges of data collection, the conversation examines how involvement in a study impacts on disease states and...

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LifeSci Talks COA Series | Exploring the Intersection of Clinical Practice and Entrepreneurship: Technological Innovation in Clinical Research

In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Dr Michelle Longmire, CEO of Medable, to discuss her journey from clinical practice to entrepreneurship, driven by a passion for rare disease, and the need for technological innovation in clinical research. The conversation highlights key challenges faced in transitioning from academia to entrepreneurship, and the importance of storytelling in...

eCOA LingCert

Access end-to-end consultation, from licensing to electronic clinical outcome assessment (eCOA) migration, and improve the patient and healthcare provider experience with all types of COAs. ...

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6 Pathways to Take Your MT Strategy to the Next Level in 2024

With 2024 well underway, innovators in the global life sciences and pharmaceutical industries continue to question how to maximize efficiencies and reduce complexities in clinical and regulatory content development and localization. As part of the broader technological roadmap, AI and automation remain front and center as key players in taking these workflows to new heights. Machine translation (MT) is expected to directly impact and transform approaches to multilingual...

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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. ...

The Ultimate Clinical Translations Checklist

Study teams who can better anticipate their language needs can better control for the abovementioned pain points. The Ultimate Clinical Trial Translations Checklist was created to help you plan for all your potential language requirements....

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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...

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C3 Summit Princeton 2024

Join your industry peers for Conversations on Clinical Content, C3 Summit. Panels of pharma, biotech, CRO, and regulatory thought leaders will explore patient diversity, centricity, and outcome assessments, discussing challenges, opportunities, and strategies through the lens of real-world experience. Take away practical insights and participate in a discussion during the Q&A and post-event cocktail hour. ...

Sign Up for Free Office Hours

Address challenges in clinical development, regulatory compliance, and patient engagement with an expert. TransPerfect Life Sciences offers a unique opportunity for free consulting through office hours with our subject matter experts. Explore some of your most pressing questions, without the cost or sales pitch. ...

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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...

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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...

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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...

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Personalized Pathways: Building an Omnichannel Ecosystem for Life Sciences

In an increasingly globalized digital landscape, the demand for personalized content has never been greater. Join Joy Wendelken from Johnson & Johnson alongside Sara Green of WebMD Ignite in conversation with Dana Weber from TransPerfect Digital as they discuss how omnichannel marketing is helping pharma companies better engage and more effectively reach patients and HCPs.You’ll hear about:• The importance (and challenges) of tailoring content in an era of information...