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Global Regulatory Compliance Support Across 120+ Countries
We help you take your innovations and products to intended users in global markets through evidence based, regulatory intelligence driven, tech assisted, seamless regulatory services. With Artixio, you gain access to over 350 regulatory experts in 120+ countries with decades of experience in successfully supporting products across diverse categories, therapy areas and complexity.
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India
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Philippines
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Japan
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Regulatory Affairs Solutions For
Markets Worldwide
We help life sciences companies comply with complex regulatory requirements in every region — with local insight and global coordination.
Artixio offers regulatory affairs support in over 120+ countries — spanning North America, Europe, Asia-Pacific, Latin America, and the Middle East. Whether you’re launching a new product or expanding into new markets, our experts understand the nuances of regional regulations and liaise directly with local Health Authorities to ensure speed, accuracy, and compliance.
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Regulatory Affairs
Product Registration
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IND (Investigational New Drug)
NDA (New Drug Application)
Regulatory Operations
Technical Writing
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AI-Driven Compliance Services
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Pharmaceuticals
MedTech
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Nutrition
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Insights from Artixio - Tips & Articles
Thailand Government Schemes for
Pharmaceutical and Medical device industries in Thailand are growing to meet the increasing demand...
Mexico COFEPRIS Updates on
Overview of December 2025 Regulatory Changes in Mexico Low risk Medical Device listing, application...
Orphan Drug Designation in
Orphan Drug Designation (ODD) is regulated by Ministry of Food and Drug Safety (MFDS)...