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Merry Christmas and Happy New Year!
Merry Christmas and Happy New Year!
Merry Christmas and Happy New Year from the Qmed Consulting team.
It has been a great 2016 and the business has experienced rapid expansion during this period. Our business objective is to enable better health from idea to revenue for our international and local clients.

In order to meet this objective we have expanded the geographical scope of our business including employees across five countries – Denmark, Switzerland, Netherlands, UK and Finland. Our clinical, regulatory and commercial health teams are now better positioned to support our clients gaining approval for new medical device technologies in Europe.

It is our pleasure to introduce you to the following new team members:

Started in November 2016:
Mark O’Reilly – Director of Business Development & Sales
Mark has a Bachelor of Science degree in Analytical Chemistry from the University of Leeds. He has over 20 years of experience in business development roles within the pharmaceutical and medical device industries. He has spent the past 10 years working in business development and market strategy for clinical, regulatory and consulting business units exclusively within the medical device market.

Mark is based in the UK and he is responsible for leading international business development, sales and marketing activities at Qmed Consulting. Read bio...

Starting in January 2017:
Puk Stewart – Senior Clinical Research Associate
Puk is a trained medical laboratory technician with a diploma from Glosburg University Hospital. She has over 19 years' experience in clinical research including roles with hospitals, pharmaceutical and medical device clients such as GE Healhcare, Amgen, MSD, Norma, Lundbeck and Inventiv health. In her most recent role she was an international clinical trial manager supporting Leo Pharmaceuticals global studies. Puk starts in January 2017 and will be based at our head office in the Copenhagen area.

Francois Redelsperger – Regulatory Affairs Specialist
Francoise has a PhD in Virology from University Denis Diderot, Paris.

Over the past 6 years he has managed several collaborative research projects involving both academic laboratories and hospitals. More recently he was involved in the national management of international vaccine clinical study.

Francoise will be joining our regulatory team and will be based at our head office in the Copenhagen area.

Helle-Maj Klint Moller – Clinical Trial Assistant
Helle-Maj has 20 years of experience within the medical industry, with the last 10 years in the medical device industry.

As Technical Designer in a hospital, she was responsible for construction projects including all documentation needed (technical drawings, time schedules etc.) and contacts with crafts.

In the medical device industry, she was responsible for CE marking of production equipment of medical devices, as well as technical documentation (manufacturing drawings, risk assessment, operators manual etc.), Quality documentation and order management on medical devices.

Qmed Consulting has transformed from a private limited company to a public limited company.
Qmed Consulting has changed its legal entity from Qmed Consulting ApS to Qmed Consulting A/S in line with business legislation in Denmark. This change will not have any implication for our current customers.

Looking forward to working with you all in the New Year.
From idea to revenue, Qmed Consulting is your partner for medical device CRO services.
Qmed Consulting A/S
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