Front

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All your post market surveillance activities at one place

Ranging from literature monitoring and individual case safety reports to aggregate data reports, we will help you to ensure compliance with MDR 2017/745.

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Shared experience

Rely on a professional team for all your case processing and literature assessment activities. Take advantage of our network of experienced medical advisors.
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Accelerate your medical device development

Through our aggregate data evaluation, facilitate development of your product portfolio. Use the acquired data in the best possible way.

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Committed to sustainability

We are dedicated to make responsible choices that balance economic, environmental, and social considerations, for a better future for all.

Our Services

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Medical device Post market surveillance

Be part of a systematic surveillance and data collection process to capture all the data pertinent for improvement of safety and performance of your products.

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Data processing

Our team can process all the data gathered through PMS activities whether it relates to quality complaints, ICSRs or literature articles. We have a multidisciplinary team to ensure quality assessment of information and in a timely manner.

aggregate data reports

We can help you ensure compliance with MDR 2017/745 with our medical writing department. Our advanced tools combined with experience will ensure that data is evaluated in the best possible way.

Clinical Solutions

With a multidisciplinary team we can aid you in the preparation clinical evaluation reports and conduction of post-market clinical follow-ups.

Adjusted to your therapeutic area

Medical device industry involves many different therapeutic areas. Our broad network of dedicated healthcare professionals and experts in their field stands at your disposal.

Focus on things that matter

Safety

Detect key safety aspects of your product for better understanding of the risk-benefit profile of your product.

Performance

Enhance performance of your products to improve safety and mitigate the risks.

Usability

Make work of healthcare professionals easier with continuous improvements to usability of your products.

Improved performance

Market-leading solutions

In line with industry standards we use the most advanced tools available on the market. For efficient detection of trends and important safety information data is analyzed quantitatively and qualitatively.

Streamlined process

Simplify the way post market surveillance is performed and focus on things that matter

Multidisciplinary approach

Whether you need clinical expertise, benefit risk assessment or statistical evaluation, rely on experts in their field to address all your specific needs.