Comprehensive Medical Device Testing Services
Your Partner for Comprehensive Medical Device Testing Services
In a market with tight timelines and stringent compliance regulations, emerging medical device manufacturers face an uphill battle to bring their products to the marketplace.
Often, manufacturers are faced with testing providers who offer “siloed” services for testing, making it necessary to find multiple testing partners to get all of the necessary compliance approvals for a medical electrical device.
Who needs those hassles?
Eurofins E&E North America offers the most comprehensive solution for medical device testing in the world. No other testing, inspection, and certification provider has the ability to meets as many medical device testing needs as Eurofins.
All Your Testing Needs Under One Umbrella
Through the vast Eurofins network of testing laboratories, we are able to provide you with a true “one-stop shop” for your medical electrical device testing needs.
We can eliminate many of the headaches and hangups that occur when dealing with several different testing labs:
|Signing/executing multiple Non-Disclosure Agreements (NDAs) and all the associated red tape that ensues|
|Having and keeping track of multiple Points of Contact (POCs) to get information and updates|
|Facilitating and monitoring multiple testing schedules, and dealing with the domino effect if one schedule changes|
|Shipping your product to multiple locations, knowing where it is at all times, and hoping it gets from one place to the next|
We can provide the services you need and the peace of mind you want.
Our Comprehensive Medical Device Testing Services comprise the following:
With more than 100 years of product safety and electromagnetic compatibility expertise, Eurofins E&E North America can help you navigate complexities in medical device compliance. From testing & certification to global market access, we help you bring your product to market faster and more cost-effectively.
With testing and regulatory expertise across >20 labs worldwide, Eurofins Medical Device Testing can help develop and execute your test plans, and navigate the regulatory pathway to market anywhere in the world while delivering a true local laboratory experience.
Our facilities maintain quality systems compliant with cGMP, GLP and ISO 17025, and conduct testing in accordance with ISO, ASTM, ANSI, ISTA, AAMI, AAALAC standards, as well as custom test methodologies to meet our customers’ unique challenges. With the highest level of instrument technology available in the industry, Eurofins Medical Device Testing has always utilized the most state-of-the-art instrumentation to deliver accurate and timely test results for more than 40 years.
EAG Laboratories has over 40 years experience in materials testing services. We support over 4,000 clients in 20+ facilities located in the United States, Europe, and Asia.
EAG is IP secured and ITAR registered, and is accredited & certified across multiple industries & markets.
Eurofins operates as a Notified Body authorized to issue EC certifications in accordance with the appropriate CE marking Directive; MDR 2017/745, MDD 93/42/EEC or IVDD 98/79/EC.
Eurofins has three designated notified bodies—n.0477, n.0537 and n.0681—for CE certification in accordance with the MDD (93/42/EEC), one for CE certification (n. 0537) in accordance with the MDR (2017/745) and one under 98/79/EC for in-vitro diagnostic medical devices directive.
Our testing and notified body services are supplied through our worldwide network of Eurofins E&E laboratories, including tests on non-active medical devices.
With more than 47,000 employees across more than 800 sites in 50 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services. Few testing laboratories can match the level of expertise, technological leadership, attention to quality, and customer service that have made Eurofins a global leader in the testing, inspection, and certification industry.