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April 03, 2017 "A comparative view on medical device regulations - When West meets East"

A comparative view on medical on device regulations- When West meets East" a Qserve article - is featured in Law View Partners' quarterly newsletter!

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February 15, 2017 Announcing Gert Bos as member of the RAPS Board of Directors

We are pleased to announce the appointment of Gert W. Bos, PhD, FRAPS, executive director and partner at Qserve Group as a new member of the RAPS Board of Directors.

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January 25, 2017 First EU MDR workshop was a success and all speakers for the February Clinical session are confirmed

On the 16th of January, 2017 the first Qserve EU MDR workshop took place in Amsterdam, The Netherlands. We were very pleased with the positive responses that were submitted through evaluations.

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January 24, 2017 Wiebe Postma, an experienced Clinical researcher joins Qserve Clinical team

It is with pleasure that we introduce Wiebe Postma as a member of our expanding team of experts. Wiebe brings experience in clinical evaluation and clinical investigation (CRO) and will join us to strengthen the Clinical Evaluation Business area, supporting also the growing need for clinical data in the field.

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January 23, 2017 Qserve expands its clinical services by offering Clinical Investigation (CRO)

The regulatory requirements regarding Clinical Evaluation have become more strict and prescriptive under the MEDDEV 2.7.1/ rev 4 and the new Medical device regulation in the EU.  Read more

January 19, 2017 Mindy McCann, an experienced Regulatory Compliance expert joins Qserve as a Principal Consultant

To futher strengthen our growing team of experts and increase presence in the US, Qserve is happy to welcome Mindy McCann to its team. Mindy brings many years of industry and Notified Body experience in Regulatory Compliance, Quality and Clinical.

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December 20, 2016 MEDDEV 2.7.1 Rev. 4 webinar in the top 5 of popular Medical Devices Webinars


The webinar "Understanding the Changes in MEDDEV 2.7.1. REV 4"  by Keith Morel, VP of Regulatory Compliance at Qserve Group is in the top 5 of most popular free Medical Device Webinars of 2016 at greenlight guru.

 
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December 13, 2016 More speakers confirmed for our 2017 MDR workshops!

We are happy to have Philippe Soly, Director of Regulatory Affairs at Philips Healthcare on the 16th of January, Benjamin Hagendorn, Head of R&D Regulatory Affairs at Merz on the 26th of June and Sophie Tabutin, Notified Body Regulatory Lead at Bsi on the 16th of October as a speaker at our upcoming EU MDR Compliance workshop program 2017. 

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November 17, 2016 MEDICA 2016: International world of Medical Device innovation and market access

The MEDICA, the largest European trade show for medical device manufacturers, is an international meeting point for the professionals in the medical Device industry. 

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November 09, 2016 Qserve Group introduces Iris Verboven at the MEDICA tradeshow in Düsseldorf

The MEDICA, the world's leading trade fair for medical industry, 14-17 November in Dusseldorf.

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