Driving Digitization and Innovation in Clinical Trials: Reducing the content burden

Life sciences and healthcare organisations face significant challenges in managing cross-border communication effectively. Ensuring patient safety, regulatory compliance, and timely market entry are critical priorities. On 25 March 2025 industry professionals uncovered strategies for improving the management of multilingual marketing, clinical, and regulatory documents when they joined this webinar, you can watch the recording here.

Key Takeaways:

• Identify the key challenges in managing cross-border marketing, clinical, and regulatory documents, and understand their impact on efficiency and compliance.
• Learn how to select and implement the right tools and processes for managing multilingual content in an efficient and compliant manner.
• Explore the potential of AI-driven MT to streamline translation processes and reduce time to market while maintaining quality and compliance.
• Outline the essential language services that ensure clear, accurate, and patient-focused communication throughout the clinical trial lifecycle.
• Hear expert perspectives on integrating linguistic technology into your existing processes to improve outcomes and efficiency.