UL Solutions ComplianceWire® Rolls Out Enhanced Features for Life Sciences GxP Training and Qualification Management
New and upgraded learning management and training features to support pharmaceutical, medical device and biotechnology companies
CH Rep Services for Medical Device Companies
CH Authorized Representative services to help medical device companies navigate local regulatory requirements to sell their products in Switzerland.
Malaysia Authorized Representative
Emergo by UL offers authorized regulatory representation for medical device companies looking to sell in the Malaysian market.
RAMS® Top FAQs
Get answers about registering, renewing accounts and what tools you’ll find in RAMS.
Software Simplifies ANVISA, COFEPRIS Regulatory Approval Process
New Emergo by UL software guides you, step by step, through the complex regulatory requirements of these two markets crucial to success in Latin America.
Medical Devices Regulation (EU MDR) Training for Manufacturers
Prepare your team for the regulations and requirements for medical device manufacturers with our on-site and remote EU MDR compliance training courses.
IVD Registration and Approval Consulting
IVD registration and approval consulting in Europe, Australia, Canada and other major medical device markets. Read more on IVD consulting.
On-Site Medical Device Single Audit Program (MDSAP) Training for Manufacturers
Become familiar with country-specific requirements, industry-related terms and what to expect from an MDSAP certification with our on-site MDSAP training.
EU Medical Device Vigilance and Incident Reporting
Learn how we can assist with European medical device vigilance and adverse event reporting, FSCA reports, post-market monitoring and creating vigilance procedures.
Medical Device Vigilance Reporting in Taiwan
Emergo by UL can help you implement a vigilance system for adverse event reporting, recalls and post-market monitoring as required by the TFDA.