Global Regulatory Writing & Consulting (GLOBAL) Employee Directory

Biotechnology ResearchWashington, United States11-50 Employees

Global Regulatory Writing & Consulting (GLOBAL) operates within the biotechnology research space, offering specialized consulting to support regulatory programs for drug and device development. Its core services include regulatory strategy, authoring for clinical trials and marketing applications, lifecycle management, submission project management and publishing, and medical writing for pre- and post-market deliverables across clinical and non-clinical domains. The organization frames its service model around tailored solutions and close collaboration, drawing on expertise typically associated with large CROs while acting as a smaller, agile partner.

Based in Tukwila, Washington, GLOBAL serves life sciences companies needing regulatory documentation and submission support across languages and geographies. It positions itself as offering the resources of a large CRO while maintaining the close collaboration typical of a smaller firm. In May 2026, GLOBAL announced a strategic partnership with Vistatec Life Sciences to help bring regulatory documentation to market faster and with improved accuracy and cross-language compliance.

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