Accelerate your medical device go-to-market in light of the new MDR

Enforceable since May 26, 2021, the Medical Device Regulation (MDR) imposes manufacturers to justify additional evidence on the efficiency and safety of their medical devices, to obtain or maintain their CE marking.

Keyrus Life Science can help you:

  • Take full advantage of the extended transition period

  • Accelerate the compliance upgrade of your existing device portfolio

Download our full brochure for more info

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We lead your R&D projects to the market

Regulatory Strategy

Optimize your research & development strategy

Thanks to our extensive clinical and regulatory expertise, specialized on the medical device challenges.

Data Viz

Maximize the success of your investigations

By choosing the right study design and entrusting them to an experienced partner.

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Rely on specialized expertise in medical devices

Trained to MDR and ISO 14155 & 14971 standards, our clinical and regulatory experts help you optimize your CEP.

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Be guided through the regulatory maze

And rely on our +25 years clinical expertise for your investigations

to secure the CE marking for both your new & existing medical devices.

Contact Us

Keyrus collects your data to process your registration and for commercial prospecting purposes. Fields marked with an asterisk are mandatory. To learn more and exercise your rights, please refer to our Privacy Policy.
Expert Opinion

Our recommendations to get the most out of the extended transition period

Read our expert opinion on the Medical Device Regulation.

Read more
We let our experience speak for itself

Keyrus Life Science accelerates the compliance process for an industry leader for their medical device product portfolio.

Faced with a shortage of regulatory and clinical experts capable of preparing submission application, our client had to ensure product compliance for its product portfolio in order to be able to continue commercialize them.

Learn more
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The Connected CRO
 With more than 25 years of experience, Keyrus Life Science makes data matter to address the biggest clinical challenges for clients around the global to enable long-term success.
 
As part of the Keyrus Group, we connect CRO expertise, life data science and digital enablement to improve clinical trial efficiency and agility, to the utmost benefit of society and human health.
 
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Human Data

We use our scientific and technical expertise to empower our clients with actionable data-driven insights.

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Inspirational Reality

We implement solutions that solve current challenges while also looking ahead at future opportunities for innovation and progress.

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Simplex Future

We’re experts at tackling complex problems and providing our clients with straightforward, effective and scalable solutions.

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