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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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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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Nutraceutical Regulation and Registration in Australia (TGA)

Nutraceutical Regulation and Registration...

In Australia, products categorized as 'complementary medicines' encompass...

March 21, 2025
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Australia (TGA) Medical Devices Regulations and Registration Process

Australia (TGA) Medical Devices...

Medical device is an instrument, apparatus or machine...

March 21, 2025
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Pharmacovigilance In Clinical Trials

Pharmacovigilance In Clinical Trials

Clinical trials are an integral part in the...

March 20, 2025
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NADFC Regulation of Nutraceuticals in Indonesia

NADFC Regulation of Nutraceuticals...

The nutraceutical market in Indonesia is expanding, with...

March 20, 2025
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Medical Devices Regulations & Registration In Indonesia

Medical Devices Regulations &...

Although the manufacturing sector for medical devices in...

March 20, 2025
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NADFC (BPOM) Regulations of Infant Formula in Indonesia

NADFC (BPOM) Regulations of...

Indonesia’s large population, coupled with a relatively high...

March 20, 2025
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EMA’s Clinical Trial Regulations (EUCTR) in European Union

EMA’s Clinical Trial Regulations...

The new EU Clinical Trial Regulation (CTR) 536/2014,...

March 20, 2025
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Understanding the Role of PRRC under EU MDR and IVDR

Understanding the Role of...

The advent of the EU Medical Device Regulations...

March 20, 2025
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Conformity Assessment of Medical Devices under EU MDR

Conformity Assessment of Medical...

The world of medical devices is a realm...

March 20, 2025
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