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Uncomplicate Your Compliance

Changing regulations are bringing new challenges to your market.

Get advice and expertise without interrupting operations.

The EU’s new Medical Device Regulation Date of Application has finally arrived, and the countdown begins for previous certificates set to expire. The latest MDR includes expanded linguistic requirements for industry content and thus can threaten to bog down your business. Further recommendations from the Medical Device Coordination Group (MDCG) are expected to be released in 2021, meaning even more for your compliance teams to absorb.

Rather than burden your teams with constantly evolving requirements, reach out to our Life Sciences team. From professional linguists to experienced scientists, we stand at the ready to update and translate your content to keep it compliant at every step.

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10+ Million

words translated


average projects per client


of projects are delivered on time

MDR Services

Device Lifecycle Language Services

From concept to customer, your medical device development needs a language partner that understands regulations across geographies and cultures. We can support compliance efforts through localization that is ongoing, saving you time and money on incremental changes you implement at any time.

Regulatory Updates

Our experts are always up to date on the latest rules and regulations. With Europe-based teams as part of our 26-country footprint, Lionbridge can work with you on your schedule no matter where you’re based.  

Meet Our MDR Experts

Pia Windelov

As the Director of Product Strategy for Lionbridge Life Sciences, Pia brings 15 years’ experience in R&D in the pharmaceutical, CRO, and MedTech sectors.

Mark Aiello

With an extensive regulatory background, Mark partners with customers to bring life-saving products to market while meeting and exceeding regulatory standards.

Related Articles

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The MDR applies across the lifecycle of devices produced, marketed and distributed through the EU. As a result, the linguistic requirements are many. Partner with Lionbridge to simplify your clinical investigations.

Post-Market Surveillance Under MDR

The EU MDR increase the linguistic burden on post-market surveillance activities. What do the new regulations mean and how can manufacturers simplify their response? Lionbridge is here to help.

Medical Device Implant Cards Under MDR

Included in the new MDR are updated requirements for implant cards. What sort of information is necessary under the latest changes?

Clinical Investigation Applications Under the MDR

Despite some harmonization, country-level regulations still apply to Clinical Investigations. Learn how the Medical Device Regulation alters language requirements and how new guidance can help you prepare for EUDAMED.

Multilingual Content Centralization for Smooth MDR Implementation

What questions to ask about your business, your products and your language services providers to thrive under the new MDR.

Competing Priorities: MDR Readiness in the Pandemic

The importance of the EU market and the lifecycle of device content. 

Lionbridge EU MDR Readiness Webinar

Listen in on a conversation between life sciences experts Pia Windelov and Mark Aiello.

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