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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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Unlocking the Power of AI and Machine Learning in Life Sciences

Life sciences companies are putting artificial intelligence (AI) and machine learning (ML) into practice, realizing its potential to revolutionize adverse event detection, diagnostics, and more. For AI and ML to be truly effective, you need to give context to your data, teaching the systems to analyze information and improve processes. This is done through data annotation. Discover immediate steps to leverage the power of AI/ML and easy solutions to get you started in this...

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C3 Summit London 2024

C3 Summit (Conversations on Clinical Content) is part of a series of events that offers sponsors, CROs, and biotech professionals opportunities to share knowledge, gain industry insights, and network. The series has been celebrated for its casual yet informative format and time-efficient, well curated discussions. Previous panels have featured topics such as inclusivity and diversity in patient recruitment, practical applications of AI/ML, regulatory inspection stories 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...

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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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An Overview of Generative AI and Machine Translation for Life Sciences

Global life sciences companies are realizing the potential artificial intelligence (AI) and machine learning (ML) has to drive efficiency in content and translation management. To capitalize on this, organizations need to identify the right solutions. Discover important considerations for integrating AI and ML into translation management strategies, steps to get started, and a practical use case in this overview....

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Multilingual Labeling: Considerations for Efficient, Cost Effective and Compliance Labeling

Accurate and compliant labeling of an investigational medicinal product (IMP) is an important and integral part of clinical trial operations. A misstep in labeling can lead to significant delays, affecting the entire study’s timeline and potentially incurring costs ranging from $100,000 to $700,000 in hard expenses. In worst-case scenarios, incorrect labeling might necessitate a complete product reproduction. Learn more about the strategies and solutions leading sponsors are...

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Engaging Patient Communities: A Pathway to Clinical Trial Success

In this webinar, the expert speakers will focus on the critical role of patient communities in advancing clinical trials. They will explore best practices for engaging with patient communities to enhance recruitment, retention and overall success of the trial. Based on case studies and interactive discussions, attendees will learn how to build trust, foster communication and address the unique needs of patient communities. In a recent study, 91 percent of sites stated they...

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AI & MT "Ask an Expert" Office Hours: Real World Data

Welcome to TransPerfect Life Sciences' AI and MT Ask an Expert Office Hours. In these sessions, we provide an opportunity for our community to submit their pressing questions for our experts to answer live, in the company of your industry peers. If you are looking for some more insight without spending money or engaging in direct sales conversations, this is a great way to explore some of your most pressing questions.   ...

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AI and MT "Ask an Expert" Office Hours": Clinical and Regulatory Documents and Content

Welcome to TransPerfect Life Sciences' AI and MT Ask an Expert Office Hours. In these sessions, we provide an opportunity for our community to submit their pressing questions for our experts to answer live, in the company of your industry peers. If you are looking for some more insight without spending money or engaging in direct sales conversations, this is a great way to explore some of your most pressing questions.   ...

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AI & MT "Ask an Expert" Office Hours": PV and Safety

Welcome to TransPerfect Life Sciences' AI and MT Ask an Expert Office Hours. In these sessions, we provide an opportunity for our community to submit their pressing questions for our experts to answer live, in the company of your industry peers. If you are looking for some more insight without spending money or engaging in direct sales conversations, this is a great way to explore some of your most pressing questions.   ...

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Trial Interactive Customer Summit, OpTImize

Join us for the inaugural OpTImize Summit, the first Trial Interactive customer event brought to you in partnership with GlobalLink NEXT. This invitation-only conference offers networking opportunities, product showcases, insightful client success stories, and thought-provoking sessions featuring Trial Interactive experts and guest speakers. ...

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AI and MT for Regulatory and Clinical Content Office Hours - 5/15/24

Welcome to TransPerfect Life Sciences' AI and MT Ask an Expert Office Hours. In these sessions, we provide an opportunity for our community to submit their pressing questions for our experts to answer live, in the company of your industry peers. If you are looking for some more insight without spending money or engaging in direct sales conversations, this is a great way to explore some of your most pressing questions....

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GL - Machine Translation Success in Life Sciences

From clinical trial documentation to patient communications and to post-market materials, machine translation (MT) enables fast, and cost efficient communication in various languages worldwide. This guide shares case studies of impactful AI and MT implementations for leading pharmaceutical, biotech, and medical device companies. Download now to see how your life sciences peers reduce translation cycle times, increase speed of global communications by 75%, and more. ...

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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Generative AI in Life Sciences Industry: Ethics, Applications, and Transformations

Discover the role of generative artificial intelligence (GenAI) in life sciences, including what is merely a trend vs. what is truly transformative. The speakers will explore pragmatic applications, ethical considerations and the potential future role of generative AI in life sciences, research and development (R&D) and product development. The discussion will provide valuable insights into the ongoing AI revolution within the life sciences sector, including practical...

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Enhancing Transparency and Safety in Medical Devices

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...