Workshop: 4 & 5 September 2017
Roundtable session: 6 September 2017
Location: Cinema-City in Glilot junction, Ramat haSharon, Tel Aviv, Israel
Price: € 900.- (Qserve does not allow entrance to conferences unless payment has been received. Delegates will be asked to pay by credit card on arrival should an invoice be outstanding).
Qserve & DEKRA have designed a 2-day high profile workshop program to assist in determining the crucial steps needed for your organization. For the attendees of the workshop, we offer the opportunity to join a Roundtable session with Gert Bos, where you have approx. 30 minutes for questions about the European MDR.
Did you know that the EU MDR is effective since the 25th of May and needs to be implemented by spring 2020, which means that the Medical Device sector needs to increase its compliance level. GAP assessment, Portfolio Analysis, Global Impact Assessment are just some of the steps on the road to EU MDR implementation that must be addressed to ensure compliance.
Speakers: Gert Bos, Executive Director and Partner at Qserve
Number of seats: Limited seats
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Who Are we? Qserve is a global medical device regulatory consulting firm. Qserve has experts in Regulatory, Quality, Clinical Affairs, and Market Access. Qserve specializes in European Regulatory issues, including the EU-MDR Compliance and MEDDEV 2.7.1 rev 4.
DEKRA, one of the top 5 Notified bodies with a local branch in Israel ever since 12 years. Currently, 9 employees work in this office. DEKRA worldwide has 33.000 employees.