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, […]
MedTech
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
Medical Devices Registration with MDA in Malaysia
The Medical Devices market in Malaysia is poised for significant growth, with projected revenue expected to reach MYR US$3,342.00m in
Medical Devices Import Regulations in India
The healthcare system that we see today has evolved and will continue to do so. Medical devices serve a major
Role of Swiss Authorized Representatives: Switzerland’s Medical Device Regulations
The Mutual Recognition Agreement (MRA) had been a pivotal instrument in fostering bilateral trade between Switzerland and the European Union
Global Medical Device Regulation: Registration Requirements
Medical devices are an unavoidable part of healthcare. Medical device development happens worldwide but not all devices are being marketed.
Government Schemes For Medical Devices In India
India holds the 4Th largest medical devices industry in India with a huge capital. India has great skills in the
Digital Therapeutics: Combining Technology for Better Health Outcomes
Digital therapeutics (DTx) are evidence-based therapeutic interventions driven by high-quality software programs to prevent, manage, or treat a medical disorder