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 | Jun 14, 2016 | Uncategorized
Medicologic has received the CIR (credit d’impôt recherche) approval by the French Ministry of Research and Higher Education as one of very few Scandinavian med-tech consultancies. Following an extensive research project in France for a leading client in the health...
by admin | Apr 7, 2016 | Uncategorized
Fredag d. 29/4 kl. 8.30 afholder Medicologic og SAXOCON et miniseminar, hvor du bliver opdateret med det seneste nye inden for såvel Medical Device Direktivet, biologisk sikkerhedsvurdering samt CE mærkning af medicinsk udstyr for in vitro diagnostik. TILMELD DIG...
by admin | Mar 14, 2016 | Uncategorized
One of the most common and internationally recognized standards for medical device quality management has been revised for the first time since 2003. We have pinpointed some of the changes and what they mean to your business.…
