This webinar will discuss the importance of thorough, accurate and timely reporting of adverse events from feasibility studies through post-market clinical trials, as well as how medical device development teams can follow best practices in using the information in product risk management
(PRWeb April 02, 2019)
Read the full story at https://www.prweb.com/releases/reducing_medical_device_product_risk_the_key_role_of_clinical_trial_data_in_product_development_upcoming_webinar_hosted_by_xtalks/prweb16210335.htm
For more information, please visit
https://www.prweb.com/releases/reducing_[...]ed_by_xtalks/prweb16210335.htm