Biopharmaceutical Alliance Launched by India, South Korea, US, Japan, and EU
The global biopharmaceutical sector has taken a significant step towards ensuring a resilient drug supply chain with the formation of […]
Artixio’s Regulatory Support for a Chinese Pharmaceutical Manufacturer in Mexico
A case study outlining Artixio’s Regulatory Support for a Chinese client: Client: Pharmaceutical Manufacturer Problem Statement A Chinese Pharmaceutical Manufacturer,
How to Use DIGIPRIS for COFEPRIS Regulatory Submissions
In recent years, companies submitting applications in Mexico have had to adjust to a different way of dealing with the
COFEPRIS Advertising Permission for Food Supplements in Mexico
If you’re a natural or legal person providing health services, beautification procedures, or promoting the consumption or sale of various
System and Procedure Packs in Accordance with EU MDR
In today’s healthcare system, the role of system and procedure packs is of great importance. Since these packs contain tools
Artificial Intelligence Impact on Global Pharma Regulatory Affairs
Artificial Intelligence (AI) has been making significant strides across various sectors, and the pharma industry is no exception. One area
Registration of Biologics in Malaysia (NPRA)
Biologics have emerged as a significant treatment for various diseases in Malaysia. With their increasing relevance in addressing chronic diseases
Thailand Medical Device Regulations & Registration Process
The production of medical devices in Thailand was estimated around 4.9 million U.S. dollars in 2022. The total market size
FAQs: Malaysia MDA Regulations for Medical Device Registration
Here are answers to some of the Frequently Asked Questions (FAQs) about Malaysia regulations for Medical Device registration. MDA Registration