Uncomplicate Your Compliance

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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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Key Facts

10+ Million

words translated

30+

average projects per client

99%+

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

Transparent Lion mark for copyright project

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.

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Lionbridge EU MDR Readiness Webinar

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

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