The Big Beautiful.... Repository!
The Global Access Regulatory Repository (GARR) is a centralized, country-organized portal of regulatory information designed to support global drug and medical device registration activities. Regulatory content is structured into country-specific Repository Cabinets, arranged alphabetically using the ISO 3166 Alpha-3 country code standard, ensuring consistency, clarity, and ease of navigation across jurisdictions.
Each Repository Cabinet provides a wide spread collection of authoritative regulatory resources, including direct links to official application forms, submission templates, and regulatory guidance documents relevant to that country. These resources are curated to help regulatory professionals efficiently plan, prepare, and execute submission and registration projects.
GARR content is continuously updated, with new countries and regulatory materials added on an ongoing basis to reflect evolving regulatory landscapes. Rather than spending hours searching across multiple agency websites, GARR enables regulatory affairs professionals to access trusted information quickly and confidently—so they can focus on advancing their projects.
Join a growing community of regulatory professionals who are working smarter, not harder, with a single, structured gateway to global regulatory information.
Faster Submission Preparation is Truly What You Know!
Access Regulatory Guidance Documents, Forms, Templates, and Links to information you need to streamline drug, device, and biologics registrations, all in one place!
