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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.

Popular Articles

Articles On Pharmaceuticals

Drugs vs Medicines: Understand The Key Differences

Drugs vs Medicines: Understand

You all might always get confused the difference between drugs and medicine....

October 4, 2025
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Vietnam Pharmaceutical Regulations & Drug Registration Process

Vietnam Pharmaceutical Regulations &

Vietnam is the 7th fastest growing middle-class population in the world and...

October 26, 2025
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NADFC (BPOM) Pharmaceuticals Regulations In Indonesia

NADFC (BPOM) Pharmaceuticals Regulations

Pharmaceutical sector is expanding day by day to occupy solutions for new...

January 5, 2026
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Medical Devices Regulations in European Union (EU MDR)

Medical Devices Regulations in...

EU MDR defines the conditions under which medical...

February 4, 2026
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Pharmaceutical Regulations in European Union

Pharmaceutical Regulations in European...

Many regulatory delays in European Union happen not...

February 4, 2026
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System and Procedure Packs in Accordance with EU MDR

System and Procedure Packs...

In today's healthcare system, the role of system...

February 4, 2026
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Artwork Proofreading & Quality Check for Top-50 European Biopharma Clients

Artwork Proofreading & Quality...

Artixio is helping pharmaceutical companies with their artwork...

February 4, 2026
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Conformity Assessment of Medical Devices under EU MDR

Conformity Assessment of Medical...

EU MDR places clear responsibility on manufacturers to...

February 4, 2026
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Regulations of Reusable Medical Devices under EU MDR

Regulations of Reusable Medical...

The introduction of the EU Medical Device Regulation...

February 4, 2026
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Role of Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU

Role of Qualified Person...

If you are responsible for placing a medicinal...

February 3, 2026
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EU MDR Labelling Requirements For Medical Devices

EU MDR Labelling Requirements...

Labelling under EU MDR is no longer something...

February 2, 2026
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Combinational Drugs Approval Process in Thailand

Combinational Drugs Approval Process...

The combinations in Thailand play a major role...

January 30, 2026
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