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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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Articles On Pharmaceuticals

AI Solutions For Pharma (From Regulatory Affairs to Custom Software)

AI Solutions For Pharma

As the technology is reaching its heights, new innovations like AI can...

September 1, 2025
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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...

July 28, 2025
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Pharma Manufacturing Booms in Hidalgo, Mexico

Pharma Manufacturing Booms in

Once overlooked pharma hub in Mexico's Hidalgo region has gained importance with...

June 18, 2025
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Responsibilities of Indian Authorized Agent for Medical Devices Import

Responsibilities of Indian Authorized...

An Indian Authorized Agent is an intermediate between...

July 30, 2025
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CDSCO Medical Device Approval Cost & Fee Structure

CDSCO Medical Device Approval...

Central Drug Standard Control Organization (CDSCO) is the...

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

Computer Software Assurance(CSA) In...

Under 21 CFR part 11, it is required...

July 28, 2025
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Virtual Reality (VR) and Augmented Reality (AR) in Pharmaceuticals

Virtual Reality (VR) and...

Virtual Reality (VR) is a virtual world with...

July 15, 2025
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IVD Medical Devices Registration & Approval In India

IVD Medical Devices Registration...

IVDs in India are regulated as drugs under...

July 8, 2025
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Product Classification Application with Ministry of Health and Prevention (MoHAP), UAE

Product Classification Application with...

For bringing any pharma product into the UAE...

July 7, 2025
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Pharmaceutical Regulation and Registration Process in Japan

Pharmaceutical Regulation and Registration...

Pharmaceuticals in Japan are regulated by the PMD...

July 7, 2025
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Biologics and Biosimilars Registration Process in China (NMPA)

Biologics and Biosimilars Registration...

Biologics and Biosimilars hold great therapeutic value, as...

July 7, 2025
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CDSCO Labeling Requirements for Cosmetics in India

CDSCO Labeling Requirements for...

The label of cosmetic products is a mode...

July 6, 2025
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