Product Classification Application with Ministry of Health and Prevention (MoHAP), UAE
For bringing any pharma product into the UAE market, it is essential to determine the MOHAP product classification and to […]
In Vitro Diagnostics: Meaning, Types And Benefits
The term “in vitro” is a Latin word that means “in glass”. Thus, from a scientific approach, we can say
Nutraceutical Regulations and Registration in Vietnam (MoH)
Nutraceuticals market in Vietnam reached USD 2.0 billion in 2024 and is projected to grow at a CAGR of ~4.5% through 2033.
Regulatory Labeling Requirements of Health Supplements in UAE
The label of a product speaks for the product. The label states what is contained in the health supplement product,
ANMAT Medical Device Regulations and Registration In Argentina
ANMAT is the regulatory authority that regulates the medical device market in Argentina. ANMAT is the Administración Nacional de Medicamentos,
Pharmaceutical Regulations and Registration in Argentina
Pharmaceutical regulations in Argentina involve stringent oversight by several authorities. At the national level, the key entities responsible for ensuring
UK Releases Amendment & Guidance on Regulations in 2024 for Medical Devices (Post-market Surveillance Requirements)
In January 2025, MHRA UK released guidance on implementation of amendments to Medical Devices Regulation 2024 regarding Post-market surveillance (PMS)
Artixio Announces Grant for Early Stage Medtech Innovators as Part of MedTech InnovateIO Initiative
HYDERABAD, India – March 27, 2024 – Artixio, a leading compliance and commercial consulting company, is proud to announce the
RFD & Pre-RFD Submissions For Combination Products In USA
The healthcare landscape is in a perpetual state of transformation, and as a consequence, there is a noticeable surge in