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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

The MD-41 and MD-42 licenses are critical components of India’s medical device regulatory framework, introduced under the Medical Devices Rules (MDR), 2017, and amended by the Medical Devices (Fifth Amendment) Rules, 2022, effective from September 30, 2022. These licenses, governed by the Central Drugs Standard Control Organization (CDSCO) and issued by State Licensing Authorities, are

Overview of EU MDR Compliance for Importers in 2026 Under the Medical Device Regulation (EU) 2017/745 (MDR), importers act as the first economic operator in the EU supply chain and bear significant responsibility for ensuring medical devices placed on the market are safe, perform as intended, and fully comply with regulatory requirements. Article 13 outlines