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Artixio

Life Science Regulatory Solutions Across Key Industries

Artixio’s multi-disciplinary team comprises of regulatory, market access and safety experts from multiple lifesciences industries. Whether it is a industry focused startup or a multi-industry products portfolio company, Artixio is a preferred go-to-market partner for leading international brands.

Serving Life Science Industries

Right from safety evaluation, regulatory strategy to commercial launch of the products, Artixio’s team has successfully managed compliance for simple ingredients to complex products in global markets.

Pharmaceuticals
Cosmetics
Nutrition
Medtech
Biologics
Veterinary

Pharmaceuticals

Our expert regulatory and market professionals have helped new molecular entities, generic drugs, radiopharmaceuticals and combination drugs with successful approval and post market safety and compliance.

Medtech

Our product categories experience range from different class of medical devices, in vitro diagnostics, software as medical devices, combination devices across application and therapy areas. 

Cosmetics

Globally leading cosmetic brands trust Artixio for expanding to new markets and ensuring ongoing compliance designed to meet the fast paced, high volume cosmetics industry.

Nutrition

Nutraceuticals, food supplements including multi vitamins, proteins, probiotics and a diverse range of innovative products have been successfully launched in global markets using Artixio’s regional presence and expertise.

Biologics

Our regional regulatory experts have led regulatory strategies for highly successful biologics products in multiple markets. Our experience spans across diverse therapeutic areas across regions.

Veterinary

Artixio continues to help both Veterinary and Animal Feed/Nutrition companies with data driven regulatory strategy and execution services right from ingredients assessment, documentation to regulatory approvals.

Our Regulatory Services

Artixio provides flexible and scalable operations services to support regulatory functions in pharmaceutical organizations. Our business models include project based support, ad-hoc requests and providing managed services through Full Time Equivalent (FTE) resources based in various locations worldwide.

Regulatory Affairs

Product Registration

Regulatory Intelligence

Technical Writing

Regulatory Staffing

Global Regulatory Outsourcing

Our Regulatory Solutions by Country

Blogs

Thailand Government Schemes for Pharma & Medical Device Industry

Thailand Government Schemes for

Pharmaceutical and Medical device industries in Thailand are growing to meet the increasing demand...

January 20, 2026
Mexico COFEPRIS Updates on Medical Devices, Tariffs & Fees(December 2025)

Mexico COFEPRIS Updates on

Overview of December 2025 Regulatory Changes in Mexico Low risk Medical Device listing, application...

January 19, 2026
Orphan Drug Designation in South Korea (MFDS)

Orphan Drug Designation in

Orphan Drug Designation (ODD) is regulated by Ministry of Food and Drug Safety (MFDS)...

December 23, 2025