Experience Global Scale and Footprint 

Leverage TransPerfect’s support in over 140 cities across six continents, providing expertise in more than 200 languages. Our global footprint ensures seamless monitoring, detection, and reporting of product effects at every site, with in-house teams ready to adapt to your unique needs.

Work with Certified Linguists

For widely used languages such as Spanish, French, Chinese, and German, machine translation (MT) can provide a fast, initial translation layer, which is then refined by expert human editors to meet the rigorous standards of global regulatory bodies like FDA, MHRA, and EMEA. This efficient and scalable approach minimizes the need for unnecessary full translations, ensuring resources are allocated strategically without sacrificing accuracy or compliance.

Expedite Responses to Regulatory Authorities

TransPerfect’s Structured Content Management System (SCMS) handles data entry, triage, and medical review processes. Optimize adverse event (AE) and serious adverse event (SAE) reporting with AI-driven automation to manage increasing data volumes efficiently. Implement risk-based workflows to focus on critical cases, expediting Periodic Safety Update Reports (PSUR) and Development Safety Update Reports (DSUR) while maintaining compliance and controlling workloads. 

Automate Pharmacovigilance Translation

Maximize efficiencies in translation accuracy, quality, and turnaround time for your PV and safety data. Harness the power of technological advancements, such as Artificial Intelligence (AI), to create a synergy between receiving, onboarding, and implementing regulatory guidance in safety workflows. By leveraging AI for fast, cost-effective translations, you can meet multilingual reporting requirements, and reduce the overall cycle times by 40%. 

Automate Literature and Social Media Review

Centralize literature and social media reviews with technology-enabled search strings, localization, and action-triggering workflows. Strengthen pharmacovigilance processes for case intake, local literature monitoring, case processing, and signal detection while boosting efficiency across your global operations.

Leverage Compliant Technology

Simplify pharmacovigilance management with our compliant solutions, including a robust pharmacovigilance system master file (PSMF) and 21 CFR Part 11-compliant eClinical tools. Ensure timely and accurate distribution of safety notification letters while adhering to Good Pharmacovigilance Practices (GVP).