Thought Leadership
Five Essential Roles Artificial Intelligence Plays in Medical Writing
Explore five pivotal roles artificial intelligence (AI) plays in streamlining and optimizing medical writing activities, including content creation, regulatory compliance, data analysis, language translation, and safety reporting. ...
C3 Summit 2023 - 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...
C3 Summit 2023 - 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...
C3 Summit 2023 - Boston
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...
C3 Summit 2023 - San Francisco
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...
LifeSci Talks COA Series | The Age of Bring Your Own Device: Considerations for Accessibility in Trial Design
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Dr. Florence Mowlem, VP of Science at ObvioHealth, to discuss maximizing patient accessibility in trial design. This includes implementing accommodations for patients...
LMS: A Must For Study Compliance And Efficiency
Life Sciences organizations function in a heavily regulated global environment, as such, have strict training requirements when it comes to investigative site staff and vendors with involvement in a study protocol. This training is necessary not only to minimize the risk of...
Maximizing Learning on a Budget: 3 Cost-Effective Strategies for Clinical Education and L&D in Medical Device Companies
Are you struggling to provide high-quality training to your clinical education and L&D teams while keeping costs low? As the medical device industry continues to evolve and grow, it’s more important than ever for medical device companies to invest in learning and development ...
Patient Recruitment and Inclusivity - The Patient Perspective
Delve into key takeaways from the C3 Summit's patient engagement panel, where industry experts and leaders discuss the challenges, opportunities, and strategies in clinical trial diversity and centricity through a candid patient perspective. Gain insights into accessibility...
Medical Device Regulation (MDR) & IVDR Timeline Overview
In order to take advantage of the MDD extension, device manufacturers must comply with several near-term deadlines and plan for long regulatory turnarounds – the extension provides less time than you might think! Learn how TransPerfect can help you meet the impending MDR and IVDR...
Harnessing the Power of Electronic Clinical Outcomes Assessments (eCOA) Technology
Digital technologies are reshaping rare disease studies, placing the question of data integrity firmly in the spotlight. In this recap from our C3 Summit Session titled Harnessing the Power of Electronic Clinical Outcomes Assessments (eCOA) Technology, we examine the impact of...
LifeSci Talks COA Series | Data Science: The New Frontier
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with Dr. Elizabeth Bacci, Senior Research Scientist at Evidera, to discuss critical aspects of developing meaningful and relevant Digital Health instruments. The...
Sponsor Strategy for Controlling Content and Language Complexity
Modern clinical trials span multiple sites and locations, requiring intense communication, documentation, and data management. As a result, many trial sites operate under a vast constellation of vendors to address patient, process, and regulatory needs, yet the external support...
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...
Anticipate Your Language Needs: The Ultimate Clinical Trial Translations Checklist
Explore the world of clinical product development and discover the pivotal role of accurate translations in global clinical trials. Empower your study teams to navigate language challenges, ensuring patient safety, regulatory compliance, and successful outcomes. Achieve these...
CCMS: A Good Fit for Pharmaceutical and Clinical Research Organizations?
Kaarin Gordon discusses the choices and challenges for efficient content reuse facing Pharmaceutical and Clinical Research Organizations. What they want is a set of tools and platforms for easy content reuse, automatic propagation of changes from a single source, and content...
Omnichannel Marketing for the Pharmaceutical Industry
With rapid globalization and expanded marketing efforts, pharmaceutical organizations are discovering that pivoting from multichannel marketing to omnichannel marketing is key to revolutionizing patient engagement. Through tailored experiences across relevant channels, your teams...
LifeSci Talks COA Series | The Future of Capturing Patient Data in Clinical Trials: DCTs, Site Staff Burden, and Regulation Considerations with Paul O'Donohoe
Mark Wade interviews Paul O'Donohoe, Senior Director of Product for eCOA and COA at Medidata. They delve into the challenges and opportunities of adopting decentralized clinical trials (DCTs) and explore topics such as mixed modalities for data capture, patient burden, site...
Walking the Tightrope: Navigating Patient Centricity and Burden in Modern Clinical Trials
Explore the evolution of clinical trials and the challenge of patient burden. Learn how to strike the right balance between patient-centricity and research data extraction....
Digitizing Multilingual COAs: A Practical Guide
Download our guide to ensuring seamless digitization of your multilingual COAs. ...
Health Canada's XML Mandate: Pioneering the Future of Pharmaceutical Content
Discover how Health Canada's transition to XML-based templates is reshaping Canadian healthcare content management. Learn about the benefits of XML formats, phases of implementation, and the transformative potential for pharmaceutical companies. TransPerfect Life Sciences...
Leveraging Technology and Bridging Gaps for Enhanced Clinical Data Management
Discover how technology-driven solutions are bridging gaps in clinical data management. Learn about challenges, trends, and strategies to enhance efficiency and streamline workflows for successful clinical research....
Transitioning Clinical Trials Under the EU CTR
The transition from Clinical Trial Directive to Clinical Trial Regulation in Europe adds new requirements and complexities to the clinical development landscape. The required transition of all trials concluding January 1st, 2025 brings about several considerations to ensure...
Driving Success in Omnichannel Content Strategies for Global and Local Markets
During our session at NEXT Pharma Summit in Dubrovnik, we explored the crucial role of an effective omnichannel approach in life sciences marketing. Seamlessly integrating multiple channels while considering the needs of global and local affiliates can unlock opportunities to...