Our team of experts has compiled case studies, white papers, process charts, guides, eLearning courses, market data, videos and additional resources for your reference.
Stay informed on emerging industry issues and deepen your knowledge of best practices, regulatory requirements and innovative technologies.
Emergo has been helping medical device and IVD companies with regulatory compliance and market entry since 1997. We maintain offices in 25+ countries, offering a wide range of compliance services, including regulatory strategy, device registration, quality
Global regulatory compliance consulting services assisting in the product lifecycle, market access, human factors research & design (HFR), and privacy and security.
We look forward to connecting with you at tradeshows around the world.
Subscribe to our newsletters to stay up to date on our latest regulatory updates and insights.
Get the latest global medical device regulatory news, insights from our experts and more.
Navigate your business in an increasingly complex world with industry-leading research and actionable insights from Emergo by UL.
Get the latest global medical device regulatory news from our experts.
Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.