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Merry Christmas and Happy New Year!
www.qmed-consulting.com
Merry Christmas and Happy New Year!
New Website
Qmed are delighted to announce the launch of our new website. We hope our new website will help you find information on specific topics or services offered by Qmed.

2019 will be a big year for the medical device community with the implementation of the new MDR. We are planning a range of topics to deliver via complimentary webinars over the year ahead. Please visit our new website and let us know if you have any comments.

www.qmed-consulting.com
On-line GCP/ISO 14115 Training course
We are currently working on developing a web-based training course for GCP/ISO 14155. This course will be launching later this month and will be available on our website. For further information please contact mor@qmed-consulting.com
Complimentary Webinars in December 2018
We are pleased to announce that we will be launching two new webinars in December.

“Software as a device under the MDR”
This webinar will address the requirements for software medical devices under the Medical Device Regulation (EU 2017/745) and propose strategies to ensure compliance.

The webinar will be delivered by Helene Quie. It will be a recorded webinar but please reach out to Mark O’Reilly on mor@qmed-consulting.com should you have any questions on this topic.

“Impact of the MDR on your technical file”
This webinar will address the proposed to changes required for your technical file under the Medical Device Regulation (EU 2017/745).

The webinar will be delivered by Johanna Horppu. It will be a recorded webinar but please reach out to Mark O’Reilly on mor@qmed-consulting.com should you have any questions on this topic.
New Employees at Qmed
We would like to welcome the following new employees to Qmed.

Bettine Jorgensen, Senior Project Manager
Bettine is a qualified nurse and as substantial experience in project management. Previously she worked as a Clinical Trial Manager for a vaccine and prior to this she worked as a Clinical Project Leader responsible for running three large medical device trials in Cardiovascular intervention and peripheral intervention. Bettine will be based at our Head office in Denmark.

Marcel Galdiers, Senior Clinical Research Associate
Marcel has a BSc in Molecular Biology and MSc in Molecular and Cell Biology. He has over 10 years experience monitoring clinical studies in Germany. Marcel also has experience of making submissions to Ethics and Competent Authority in Germany. Marcel will be home based in Germany.
From idea to revenue, Qmed Consulting is your partner for medical device CRO services.
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