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 2, 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

Asia - Contract Staffing & Hiring for Regulatory Affairs (Pharmaceuticals & Devices)

Artixio’s Contract Staffing solutions in Asia can be tailored to suit your needs and long term Regulatory Affairs strategy

Jul 31, 20232 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

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 21, 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, 202310 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

FAQ - Mexico (COFEPRIS) Regulations for Medical Device Registration

Here are answers to some of the Frequently Asked Questions about Mexico Medical Device Regulations.

Jul 9, 202310 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 7, 20236 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

Jul 4, 20238 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

Vietnam Regulations for Registration of Medical Device

In Vietnam, manufacturers and importers of medical devices must undergo a registration process overseen by the Medical Device Administration

Jun 22, 20235 min read

Expanded Access by USA FDA for Investigational Drugs

In the United States, the approval process for unregistered medicinal products under Early Access Program (EAP) is known as Expanded Access

Jun 20, 20232 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

COFEPRIS Introduces Changes to Drug Registration Process in Mexico

The Mexican health authority, COFEPRIS (Comisión Federal para la Protección contra Riesgos Sanitarios), has a new drug registration process