You will find basic demographic and healthcare market data on Mexico, plus specific information about the medical device and healthcare industries.
Greenlight Guru’s eQMS platform and ComplianceWire® compliance training and learning management system (LMS) from UL Solutions to deliver solutions for long-term success.
Read more about Mexico's federal committee for protection from sanitary risks and see the most important medical device regulations
Appoint Emergo as your registered US FDA Agent representation and learn about our responsibilities as the liaison between your medical device or IVD company and the FDA.
Learn about what Emergo by UL can provide as your TGA Sponsor for Australia and what it means for us to act as a representative for medical device and IVD companies.
Emergo by UL can help you register your medical device in Peru, including preparing and submitting the required registration materials to DIGEMID standards.
Emergo by UL can assist you with gaining medical device marketing authorization (MDMA) approval from the Saudi Food and Drug Authority (SFDA).
Regulatory compliance doesn’t end when your device goes to market. We design compliance solutions informed by a life-cycle approach to device safety and effectiveness.
Learn about the regulations surrounding Medical Device Establishment Licenses (MDEL) and the process for MDL registration and approval with Health Canada.
We conduct ISO 13485 pre-certification and FDA QSR (21 CFR 820) compliance audits for medical device companies.