Why select Emergo as your EU Authorized Representative?
Emergo Europe, a subsidiary of Emergo Group, is one of the largest EU Authorized Representatives for medical devices, representing more than 450 companies worldwide. We have built our reputation on providing friendly and fast service to our Authorized Representative clients. Because we have several offices in the USA plus offices in Europe, Canada and Australia, many device and IVD companies prefer to appoint us as their EU Authorized Representative because they know they will be able to get answers to their questions quickly. Here are more reasons to choose Emergo:
- We are a stable, ongoing business founded in 1997
- Our familiarity with the European Competent Authorities allows us to promote the best interests of our clients
- We are an ISO 9001:2000 registered firm which includes Authorized Representation in the scope of its registration
- You will receive free email updates and documents on European regulations for medical devices
- You will have secure, revision-controlled online access to all of your documentation including Technical Files, Labeling Info & Symbols, Language Requirements, Directives and more. This service is provided at no additional cost.
- We have offices in the USA and Europe, allowing you to call us with questions at nearly any US or European working hour regardless of your time zone
- We carry full liability insurance
- We offer a wide range of other quality assurance and regulatory consulting services
Please contact us for a free consultation and no-obligation proposal on EU Authorized Representative services from Emergo Europe.
Related services offered by Emergo Group:
- FDA GMP auditing and ISO 13485 auditing services
- GMP training, CE Marking training and ISO 13485:2003 training
- European Authorized Representative
- SEE ALL EMERGO MEDICAL DEVICE CONSULTING SERVICES
