Date: 13-14 July 2017
Gert Bos, executive Director, and Partner at Qserve is invited as
a speaker at European Medical Device Regulation Conference in Alexandria.
He will be giving a workshop on “Impact assessment – Identifying necessary Regulatory Revisions”:
- Determining EU MDR compliance
gaps in corporate regulatory structure
- Risk-based approach to new
rules & the regulatory strategy revision
- Engaging with other teams to
ensure all areas of impact are addressed
- Implementing a thorough &
detailed regulatory revision plan
Q1 has over a dozen years of experience in providing high level
educational content for the European Medical Device Industry and is
consistently ranked by participants as delivering quality program content,
speaker selection, and facilitation.
This program is unique in that it is specifically for global
companies based in the United States to understand the new regulatory rules in
Europe. All content is delivered by medical device industry experts, and
notified bodies as keynote panels, case studies, fireside chats, workshops, and
master classes so you will return to the office with tangible ideas that may be
The agenda of this event can be downloaded here.
More information about Gert Bos: