On the 16th of January, 2017 the first Qserve EU MDR workshop took place in Amsterdam, The Netherlands. We were very pleased with the positive responses that were submitted through evaluations. Both the presentations and the Workshop session consistently received ‘very interesting’ in the evaluations and all attendees would recommend the workshop to a colleague.
The industry professionals from Geistlich, Philips and Qserve addressed the most important topics for the steps to implement EU-MDR Compliance.
Iris Verboven, Business Development Manager at Qserve group says; “I am very happy with the positive feedback on the first EU MDR workshop session. I am looking forward to the next sessions, which will feature experienced Notified Body and Industry speakers."
We are happy to welcome Geeske van Oort, Clinical, Reimbursement & Quality Director at The eNose Company, Bassil Akra, Global Director TüV SüD, Sabina Hoekstra, Lead for European Regulation at Philips and Anna Pietersma, Principal Consultant at Qserve on the 20th of February as speakers at our session about Clinical Meddev 2.7.1. Rev 4.
Qserve has designed a monthly modular European MDR workshop program to assist in determining the crucial steps needed for your organization. Qserve’s panel of guest speakers will provide the opportunity to interact, network and discuss your organizations’ challenges, thus making these workshops unique.