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Below is a comprehensive overview of medical device regulatory affairs as it applies to medical device manufacturers. This covers key global transterritorial frameworks (US FDA, EU MDR/IVDR, and global harmonization via IMDRF), core responsibilities of manufacturers, and practical compliance strategies. 1. What is Medical Device Regulatory Affairs? Regulatory Affairs (RA) in medical devices is the

EU MDR 2026 compliance is critical for U.S. exporters of medical devices, as new import regulations, stricter CE marking rules, and updated European regulators’ oversight come into force — and ignoring them could block your products at the border. In this environment of tightening medical devices compliance and UDI/CE-marking enforcement, American manufacturers and distributors must

Breaking: EU’s 2026 Medical Device Crackdown – US Exporters Risk Billions Without These Vital Certifications Washington, D.C. pouring millions into innovative heart monitors or surgical tools, only to watch them gather dust at European ports because of overlooked paperwork. That’s the stark reality facing U.S. medical device makers as Europe’s regulatory hammer drops in 2026.

Are You Looking to Import Medical Devices into India? India’s healthcare industry is growing rapidly, and the demand for high-quality medical devices is at an all-time high. Whether you’re a hospital, distributor, clinic, or healthcare startup, importing medical devices from global markets can give you a strong competitive edge. But the process isn’t simple —

The term “TAC approval” in the context of India primarily refers to the Type Approval Certificate (TAC), a mandatory certification for automotive products under the Central Motor Vehicles Rules (CMVR), 1989, enforced by the Ministry of Road Transport and Highways (MoRTH). This certification ensures that vehicles and automotive components meet stringent technical, safety, and regulatory