Resource

Xtalks Webinar: Artificial Intelligence and Structured Data: Driving Process Efficiency for Medical Device Manufacturers

Since the advent of artificial intelligence (AI), medical device manufacturers have been early adopters for product enhancements. Now, manufacturers are evaluating their regulated content and other production processes for suitable applications of AI and automation technology. Moreover, while AI offers unprecedented opportunities for increased efficiency, accuracy and quality, it also requires a strong foundation of structured data and an awareness of global regulatory...

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. ...

XCompare - COA Migration

Reduce eCOA migration errors with XCompare technology that automates your development and translation workflows....

Resource

LifeSci Talks | Effective Rater Training: A Critical but Overlooked Part of COA Administration

In this episode of LifeSci Talks, TransPerfect Life Sciences’ Global Practice Leader Mark Wade sits down with Kelly Dumais PhD, Director of eCOA Science at Clario to discuss the significance rater training plays in standardizing the administration and scoring of clinical scales. Aiming to reduce bias and enhance data quality, you’ll hear about potential strategies for better engaging patients and how comprehensive proactive training can reduce patient and site burden. Listen...

Resource

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....

Resource

LifeSci Talks | Measuring What Matters: Modernizing Clinical Outcome Assessments with Patient-Centric Approaches

In this episode of LifeSci Talks, TransPerfect’s Global Practice Leader Mark Wade sits down with Dr. Karl McEvoy, VP of eCOA and Patient Technology at YPrime, to discuss the importance of embracing technology in clinical research to reduce the patient burden. The two cover everything from updating legacy instruments to more modern solutions such as using video assessments, to incorporating caregiver and patient advocacy groups input for reshaping trial design. Listen in for...

Resource

Lessons Learned from SCMS Deployments in Global Medical Device Documentation

Transitioning to modular content using a Structured Content Management System (SCMS) has the potential to transform medical device documentation by streamlining authoring and automating content updates and publishing. For a truly successful implementation, however, early planning and strategic alignment are essential. In this webinar, we welcome back industry experts from Bayer, Medtronic, and Carestream for an insightful discussion around how structured data, automation, and...

Resource

Sanofi’s Journey of Digital Transformation through AI-Powered Translations

The global clinical landscape is becoming more complex every day, with evolving regulations and increased pressure on life sciences organizations to reduce costs and timelines. Join us for an in-depth discussion on how one of the world’s leading pharma companies is leveraging AI to enhance their translation processes, quality, and globalization strategy across internal departments. From integrations between cloud-based translation systems and regulatory platforms to...

Resource

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...

Resource

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...