Thought Leadership
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...
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...
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...
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...
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...
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....
The Mindset Shift: Integrating Digital Strategies to Enhance Medical Affairs
In today’s evolving healthcare landscape, the role of medical affairs has been undergoing a transformation from a supportive function to a key strategic player. This shift is prompting medical teams to explore digital innovations and offer efficiencies with scaled practices. ...
Xtalks Webinar: Artificial Intelligence and Structured Data: Driving Process Efficiency for Medical Device Manufacturers
As more and more clinical trials are conducted internationally, with a higher level of protocol complexity, and with increased competition to get medical products to market faster globally, the need for efficient and streamlined clinical product development is greater than ever. ...
AI and MT for Regulatory and Clinical Content Office Hours - 10/9/24
TransPerfect's experts gather to answer questions from global pharma, biotech, and medical device leaders regarding AI and MT use cases, challenges, opportunities, best practices, and more....
Scaling Global Campaigns with AI and Human Expertise: Lessons from Sanofi
Navigating the complexities of global healthcare campaigns requires a well-balanced mix of technology and human touch. In this webinar, TransPerfect welcomes back Krista Goedel, Clinical Digital Content Lead along with colleague Lyly Fong, Global Corporate Website Manager at...
LifeSci Talks COA Series | From Interview to Endpoint: Understanding the Importance of Patient Listening to Build Better Outcomes
In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with John Reites, Co-Founder and CEO of THREAD research to discuss the importance of patient listening to build better clinical trial endpoints. They delve...
Accelerating Clinical Product Development through Centralized Content Work Streams
As more and more clinical trials are conducted internationally, with a higher level of protocol complexity, and with increased competition to get medical products to market faster globally, the need for efficient and streamlined clinical product development is greater than ever. ...
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...
E-Learning in Pharma: Creating & Managing Global Training Programs
From compliance and standard operating procedures (SOPs), to product info and sales techniques, e-learning ensures global teams have access to top-notch, consistent, and on-demand training. This guide explores key considerations for effective and engaging global e-learning...
Pragmatic Use Cases for AI in Pharmacovigilance and Safety
The rapid rise of artificial intelligence presents an opportunity for effective and transformative applications in pharmacovigilance. Intake, query routing and response, case reporting, HAQs, and more are now extremely feasible use cases that create exponential efficiency in...