This session focuses on Website Localization for Patient Recruitment. Tackle your toughest patient recruitment and engagement challenges with free, no-strings-attached advice from TransPerfect's web localization and AI experts—no cost, no sales pitch, just solutions!...
AI isn’t just a tool—it’s a transformation. See how leading medical device firms use scalable, customized AI programs to cut costs, improve efficiency, and meet regulatory demands....
From clinical trial documentation and patient communications to post-market materials, machine translation (MT) enables fast, cost-efficient communication in various languages worldwide....
Regulatory agencies worldwide, including the FDA, EMA, and other health authorities, require eCOA translations to be accurate, validated, and culturally adapted. ...
Patient recruitment is the costliest bottleneck in clinical research. Learn proven strategies to reduce study delays, optimize enrollment, and cut regrettable spend....
Meet global regulatory expectations the first time with these efficient, cost-effective, and compliant product labeling solutions and considerations....
Explore how AI enhances safety reporting, automates processes, and drives compliance in pharmacovigilance....
Future-proof your MT strategy for clinical and regulatory content with this guide....
Part of TransPerfect's GlobalLink suite of productivity applications, GlobalLink Now is a simple, but powerful way to access secure, customized AI. The system has an intuitive UI for sign on and engagement, making the application easy to use and adopt. ...
Learn how pharmaceutical companies can streamline global training programs through customizable, compliant, and engaging e-learning solutions....
Everything you need to recruit and retain patients across borders, from localization checklists to real-world case studies, in one place. Inside, you'll find audit-ready frameworks, proven recruitment strategies, and firsthand accounts of how a top 10 pharma leader expanded trial access across nine and fifteen languages. Whether you're building a global recruitment program from the ground up or refining an existing approach, these resources are designed to help your...
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. Many clinical teams have experienced delays or bottlenecks in their programs as a result of not getting accurate local-language documentation to sites quickly enough. With companies working to...
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...
Medical information teams are being asked to do more with less; faster turnaround, broader content demands, and zero tolerance for inaccuracy. AI offers a way forward, but adoption comes with real challenges: how do you validate accuracy, integrate literature review, and build governance that satisfies compliance requirements? This session brings together MedInfo leaders from Pfizer, UCB, and Elytra Consulting to discuss these questions head-on, sharing how their teams are...
