Managing Your Complaints and Obstacles in Post-Market Requirements — Results from Top Medical Device Observations During an Inspection
Managing Your Complaints and Obstacles in Post-Market Requirements — Results from Top Medical Device Observations During an Inspection : Managing Your Complaints and Obstacles in Post-Market Requirements – Results from Top Medical Device Observations During an Inspection has been organised by ComplianceOnline at Minneapolis, Minnesota, United States Date: Oct 18 - 19, 2018 Post-Market activities, Complaint Handling, MDR, and Recalls are expensive, time-consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas. Read more: https://ift.tt/2JhbcmB #medicaleventsguide #medicalevents #medicalconference #healthcareevents #healthcareconference from Tumblr https://medicaleventsguide.tumblr.com/post/177611532134