Resource

The Global Patient Recruitment Toolkit

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...

Resource

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. 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...

Resource

Xtalks | Improve Recruitment Outcomes Through More Diverse Clinical Trials

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...

Resource

AI in Medical Information: Challenges, Opportunities, and the Path to Compliant Content at Scale

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...

Pharmacovigilance and Safety Solutions

Observe, detect, and monitor the effects of your pharmaceutical products across locations and languages with translation and call services. Ensure drug safety across your entire portfolio....