Nutraceutical & Dietary supplements regulations in Mexico
Mexico's nutritional supplements market is set to expand from $9.2 Mn in 2022 to $14.96 Mn by 2030, exhibiting a CAGR of 7.4%. The...
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Aug 4, 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 3, 20234 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 2, 20234 min read
Medicines and Healthcare Products Regulatory Agency (MHRA) Pharmaceutical Regulations and Registration in the UK
In 2024, the Pharmaceuticals market in the United Kingdom is poised for significant growth, with projected revenue expected to reach...
Aug 1, 20237 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...
Jul 31, 20235 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 29, 20237 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 28, 20235 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 21, 202310 min read
FAQs – Australia (TGA) Regulations for Medical Device Registration
The regulatory authority responsible for medical device registration in Australia is the Therapeutic Goods Administration (TGA)
Jul 20, 202310 min read
FAQ - Singapore (HSA) Regulations for Medical Device Registration
The Health Sciences Authority (HSA) is the regulatory authority responsible for medical device registration in Singapore.
Jul 20, 20238 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 19, 202310 min read
FAQ - Malaysia (MDA) Regulations for Medical Device Registration
FAQ - Malaysia (MDA) Regulations for Medical Device Registration
Jul 12, 20235 min read
Pharmaceutical Regulations in Thailand
Thailand FDA Regulations for Pharmaceutical Registration
Jul 12, 20237 min read
Medical Device Regulations and Registration Process in Argentina, ANMAT
ANMAT is an Argentine regulatory authority responsible for the regulations governing registration process of medical devices
Jul 7, 20236 min read
Australia (TGA) Medical Devices Regulations and Registration Process
Medical devices in Australia shall be approved under regulations governed by the Australian regulatory authority called TGA
Jul 4, 20238 min read
United Kingdom (UK) - Medical Device Regulations and Registration Process (MHRA)
Registration process for medical devices as per regulations in the United Kingdom (UK) MHRA
Jun 28, 20236 min read
Medical Device Regulations and Registration Process in Taiwan
Medical devices regulations and registration process in Taiwan explained
Jun 28, 20235 min read
Medical Device Regulations in China (NMPA)
National Medical Products Administration (NMPA) Governs Regulations for Medical Devices in China
Jun 26, 20235 min read
Mexico (COFEPRIS) Regulations for Medical Device Registration
COFEPRIS in Mexico governs the regulations for registration of medical devices
Jun 20, 20231 min read
What are the Responsibilities of an Indian Authorized Agent for Medical Devices Import?
An Indian Authorized Agent must fulfill critical responsibilities detailed in the Medical Device Rules (MDR), 2017 to be able to import
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