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The Mexico COFEPRIS Good Manufacturing Practices (GMP) Requirements for Cosmetics
The Mexican Official Standard NOM-259-SSA1-2022 outlines comprehensive regulations covering various aspects of good manufacturing...
Oct 24, 20239 min read


Pharmaceutical Regulations and Registration in Colombia (INVIMA)
Colombia stands out for its pharmaceutical industry's ability to offer a diverse portfolio of products. Approximately half of the sales...
Aug 22, 20234 min read


Nutraceutical Registration and Regulations in the UK (MHRA): A Comprehensive Guide
The global nutraceutical industry has experienced remarkable growth in recent years, largely due to a rising consumer focus on health and...
Aug 21, 20234 min read


Biologics and Biosimilars Regulations and Registration in China (NMPA)
In China, 40% of the biologics market comprises biosimilars. The usage of biosimilars in oncology has increased as cancer overtook heart...
Aug 18, 20235 min read


Biologics and Biosimilar Regulations and Registration in Brazil
According to the Drugs Sector Regulation Chamber (CMED) in 2022, the Brazilian pharmaceutical sector generated US $17.2 billion in sales...
Aug 17, 20235 min read


Nutraceutical Regulations and Registration in Hong Kong (FEHD)
Hong Kong stands out as a dynamic hub in Asia's health supplement market. The trend of consumers embracing a diverse range of dietary...
Aug 15, 20233 min read


ANVISA Nutraceutical and Dietary Supplements Regulations in Brazil
In recent years, there has been a growing interest in nutraceuticals and dietary supplements as individuals seek to improve their overall...
Aug 7, 20233 min read


Nutraceutical & Dietary supplements regulations in Mexico
The Mexican population is seen getting very conscious about their health and early aging which has led to an increase in the demand for...
Aug 5, 20235 min read


Pharmaceutical Regulations in Japan
In the Japanese pharmaceutical industry, the journey of developing a new drug is marked by formidable challenges. Statistical data...
Aug 4, 20235 min read


Regulations for Pharmaceutical Registration in Hong Kong
The pharmaceutical market in Hong Kong has reached a significant size, estimated to be around $2.3 billion. This figure highlights the...
Aug 3, 20234 min read


Pharmaceutical Regulations in European Union
The European pharmaceutical market is expected to reach USD 432.12 billion by 2028, growing at a CAGR of 5.4%. Cancer therapeutics is...
Aug 1, 20237 min read


Medical Device Regulations in Colombia: A Comprehensive Guide
In 2023, the Medical Devices market in Colombia is expected to achieve an impressive revenue milestone of US$2.00 billion. This reflects...
Jul 31, 20235 min read


Pharmaceutical Regulations and Registration in Vietnam
Vietnam is the 7th fastest growing middle-class population in the world and aims to achieve an upper middle class income status by 2035,...
Jul 29, 20239 min read


Pharmaceutical Regulations and Registration in South Korea (MFDS)
The pharmaceutical market in South Korea was estimated to be worth 25.4 trillion South Korean won in 2021. The market size has been...
Jul 28, 20235 min read


Medical Device Regulations and Registration Process in Thailand
Medical Device Regulations and Registration Process in Thailand The production of medical devices in Thailand was estimated around 4.9...
Jul 20, 20238 min read


Pharmaceutical Regulations in Thailand
Thailand FDA Regulations for Pharmaceutical Registration
Jul 12, 20235 min read


Medical Device Regulations and Registration Process in Taiwan
Medical devices regulations and registration process in Taiwan explained
Jun 28, 20236 min read


Medical Device Regulations in China (NMPA)
National Medical Products Administration (NMPA) Governs Regulations for Medical Devices in China
Jun 28, 20235 min read


Mexico (COFEPRIS) Regulations for Medical Device Registration
COFEPRIS in Mexico governs the regulations for registration of medical devices
Jun 26, 20235 min read


New Drug Registration Process in Vietnam (DAV)
The new drug registration process in Vietnam was introduced by DAV (Drug Administration Vietnam) in October 2022
Jun 20, 20235 min read
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Deep dive and engage in insightful discourse driven by concurrent global regulatory scenarios, industry trends and Artixio’s real-time experience across the product value chain. Whitepapers, research articles, landscape reports and case studies to help you stay ahead of the curve.
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