QUNIQUE presents its seminar and workshop 'Medical Device Regulation (MDR) Performing Successful Clinical Evaluation', which will take place on the 11 January 2018 in Zurich Hilton Hospital.
Key topics will include:
Clinical requirements of medican device directives (MDD) versus MDR
The clinical evaluation process
Following good clinical practice (GCP)
Post-market clinical follow-up (PMCF) requirements and how to plan accordingly
Download this free white paper to find out more.
Thank you.Please check your email to download the white paper.