by admin | Aug 9, 2016 | Corporate, Management consulting, Quality Assurance, Regulatory affairs, Uncategorized
As part of a continued focus on delivering high-value RA/QA consulting for medical device companies, Medicologic has hired Gert Nielsen in the role as Senior Regulatory Affairs Consultant. Gert has almost 20 years of experience within Regulatory Affairs, working for...
by admin | Jun 14, 2016 | Business development, Corporate, End-to-end consulting, Quality Assurance, Regulatory affairs
On 25 May 2016, the EU agreed new rules on medical devices and in vitro diagnostic medical devices. The Netherlands presidency of the Council and representatives of the European Parliament reached a political agreement. It is still subject to approval...
by admin | Sep 3, 2014 | Business development, Corporate, End-to-end consulting, Management consulting, Medical device development, Process Management, Product development, QMS - Quality Management System, Regulatory affairs, Research & Development
1st of October 2014, we’ll be moving to our new modern office space in Ørestaden with plenty of room for both development and growth. We have in recent years experienced a significant increase in demand and positive growth within our...
