
13th Annual
EU Medical Device Clinical Research Conference
November 2022 | Location TBD
Optimize patient-centric clinical trial design that garners sufficient evidence & improves product approval
Program Overview
Implement economical clinical strategies that generate required evidence and meet compliance standards. Presenters representing various device classes share necessary measures for fulfilling clinical evaluation planning requirements including sufficient data sets. Together, attendees discuss practical methods for optimizing study design, cover expectations from expert panel reviews and dive deep into updated regulatory guidance for actionable takeaways for product approval.
Countown to the 13th Annual EU Medical Device Clinical Research Conference
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“I found the conference to be very interesting, and the quality of presentations very high level. Interactions with the other participants were also really insightful”
Severine Oudin, Clinical Writer EMEA , Integra LifeSciences
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Aaron Van Dyke
Operations Director, Life Science
Q1 Productions
312-840-9086
avandyke@q1productions.com
www.q1productions.com