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

CDSCO Medical Device Approval Cost & Fee Structure

CDSCO Medical Device Approval

Central Drug Standard Control Organization (CDSCO) is the regulatory authority that regulates Medical Devices...

July 29, 2025
Computer Software Assurance(CSA) In Pharma & Medical Industry

Computer Software Assurance(CSA) In

Under 21 CFR part 11, it is required to validate the electronic systems that...

July 28, 2025
In Vitro Diagnostics: Meaning, Types And Benefits

In Vitro Diagnostics: Meaning,

The term “in vitro” is a Latin word that means “in glass”. Thus, from...

June 20, 2025