As Global Head of Regulatory/ QA & Operations, I am responsible for identifying potential NovusLife projects that fit into our service offerings. NovusLife will assist innovative European medical device as well as rare disease firms with their challenges; especially ones having to do with entering the US (and other country) markets. Conversely, I will lead efforts for NovusLife's US clients to enter into the European market. Sample offerings include:
Regulatory and Clinical Affairs Consulting as well as marketing authorizations in EMEA, US, and Far-East regions
Interact with authorities, notified bodies and other approving bodies for fast and smooth product approval
Identify potentia...