Artixio

Global Regulatory Strategies & Expert Insights

Explore a wealth of strategic and practical insights from Artixio’s global regulatory, safety and market access teams with proven cross-functional industry experience. Discover regulations and guidelines from global health authorities, case studies, best practices and handy tips for your success in global markets.

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FSSAI Labeling Requirements For Infant Formula In India

FSSAI Labeling Requirements For

Ensuring the safety and quality of infant formula is paramount for the health and...

April 12, 2025
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Health Supplements Regulation and Registration In UAE

Health Supplements Regulation and

The world we see today is more aligned with health. They tend to be...

April 13, 2025
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Artixio Helps USA Pharma Company Register New Drugs on Time & on Budget Through Regulatory Staffing

Artixio Helps USA Pharma...

Regulatory affairs (RA) is a critical function for...

April 1, 2025
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A Case Study : Registration of Health Supplements in UAE

A Case Study :...

Navigating the complex regulatory landscape of a new...

April 1, 2025
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Case Study: Global Regulatory Intelligence for Dental Brand

Case Study: Global Regulatory...

Client: A global dental care brand headquartered in...

April 1, 2025
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Artixio’s Regulatory Support for a Chinese Pharmaceutical Manufacturer in Mexico

Artixio’s Regulatory Support for...

A case study outlining Artixio’s Regulatory Support for...

April 1, 2025
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Case Study: Enabling Product Positioning for Filtration Devices Using Primary Market Intelligence

Case Study: Enabling Product...

Client Details: Client is a large scale, multi-industry...

April 1, 2025
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Case Study: Successful Registration of Software as Medical Device (SaMD) Assisting Surgical Procedure

Case Study: Successful Registration...

Client: The client, a pioneering European company specializing...

April 1, 2025
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Pharmaceutical Packaging Graphic Design – Challenges and Remediation

Pharmaceutical Packaging Graphic Design...

Pharmaceutical companies face several key challenges when it...

April 1, 2025
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Quality System Regulations (QSR) under 21 CFR Part 820

Quality System Regulations (QSR)...

The Quality System Regulations (QSR), outlined in 21...

April 1, 2025
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eCTD Structure & Submission Process

eCTD Structure & Submission...

Common Technical Document (CTD) is a common standard...

April 1, 2025
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