Investigational Medicinal Product Labeling
Achieve faster timelines with TransPerfect Life Sciences’ ISO-certified multilingual clinical supply labeling processes for compliant, translated, and certified IMP labels for any country or language....
Local Literature Monitoring
Monitor the safety profile and of the risk-benefit balance of medicinal products, particularly in relation to the detection of new safety signals or emerging safety issues, according to the GVP Module VI requirements ...
Content Reuse
TransPerfect Life Sciences’ scalable, automated solutions for structured content authoring reduce the risk of human error in content reuse and drive down cycle times in producing and translating content. ...
Chatbots for Life Sciences
Leverage conversational AI to connect with patients and HCPs wherever they are, in whatever language they speak....
GlobalLink TMS
Reduce your cycle times and translation costs while improving resource allocation and achieving greater visibility...
Patient Recruitment Strategies: Empowering Patients Through Accessible Information
From pre-screen to post-trial, patients require clear, personalized and supportive communication to navigate the clinical trial journey. Despite the industry’s recognition of patient centricity and the abundance of digital health solutions, many trial participants still struggle to understand treatment information and access resources tailored to their needs. These gaps can lead to confusion, frustration and distrust throughout the care journey. For digital advancements to...
LifeSci Talks COA Series | Meaningful Patient Involvement in HTA Decision-making: Where do we go from here?
In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Alice Biggane, Outcomes Innovation and Research Lead at Pfizer, to discuss how PRO measures inform and impact endpoint adjudication and reimbursement decisions, due to the lack of HRQoL data included. Together they unpack other methods that can be used for augmenting the quantification with regards to HRQoL, and the complex interplay between more general Measures...
Social Listening
Gain insights into your product’s success through monitoring patient and customer feedback, conversations around your target keywords, competitors, industry topics, brand mentions, and more on global social media networks. ...
Patient Services
Deploy evidence-based patient engagement tools to increase compliance and elevate product readiness. Meet the ever-growing needs of patient-centric and inclusive solutions. ...
AI in Pharmacovigilance: A Catalyst for Progress or a Tradeoff to Human Potential?
In an environment as high stakes as pharmacovigilance, AI is not just about technology implementation; it's about balancing compliance, patient safety, and developmental breakthroughs. In this session, industry experts Dr. Siva Kumar Buddha of Amgen alongside TransPerfect's Poojah Singh will discuss how to integrate AI into existing processes in a strategic, fit-for-purpose approach. The two will discuss some of the challenges and risks associated with AI...
Life Sciences Learning Trends - Office Hours Q&A
Join the TransPerfect Learning team for an interactive virtual C3 Study Session, focused on the latest commercial learning trends transforming the life sciences industry. Whether you attended LTEN 2025 or are simply passionate about advancing learning & development in your life sciences organizations, this session is designed for you! Gain firsthand insights from Tim Robinson (Head of Learning Experience), Sarah Minkoff Stevens (Senior Learning Manager), and Gracie...
Optimizing Technology and Automation for Digital Health Products
Accurate and culturally appropriate translation of clinical outcome assessments (COAs), including patient-reported outcome measures, is essential to ensuring reliable data in multinational trials. Foundations of Clinical Outcome Assessment Localization will provide a practical overview of why linguistic validation goes beyond standard translation and how it safeguards both data integrity and patient understanding. The session will cover current regulatory guidance, the steps...
Foundations of Clinical Outcome Assessment Localization
Accurate and culturally appropriate translation of clinical outcome assessments (COAs), including patient-reported outcome measures, is essential to ensuring reliable data in multinational trials. Foundations of Clinical Outcome Assessment Localization will provide a practical overview of why linguistic validation goes beyond standard translation and how it safeguards both data integrity and patient understanding. The session will cover current regulatory guidance, the steps...
From Local to Global: How a Top 10 Pharma Leader Delivered Trial Access in Nine Languages
Discover how one of the world’s leading pharmaceutical companies made its clinical trial website accessible to global patients, but faced tight timelines, limited resources, and shifting systems. See how the team overcame these challenges to launch a multilingual site that set a new standard for global accessibility....
Opening Doors Worldwide: Launching a Top 10 Pharma’s Careers Site in 15 Languages
With an ambitious global rollout deadline and limited internal bandwidth, this top 10 pharma company needed a smarter way to scale localization. Learn how automation and streamlined workflows helped transform the candidate experience across 15 markets, without slowing down speed to launch....