Interactive Q&A July 16, 2021: Post-market Surveillance Requirements for Medical Devices
Interactive Q&A July 16, 2021: Post-market Surveillance Requirements for Medical DevicesПодробнее
Post-Market Surveillance Summary Reporting WebinarПодробнее
Interactive Q&A June 11, 2021: Post-market Surveillance Requirements for Medical DevicesПодробнее
Post-market Surveillance Requirements in ISO 14971Подробнее
Understanding Post-Market Surveillance Requirements under EU MDRПодробнее
Post Market Surveillance For Medical DevicesПодробнее
Effective Medical Device Post-Market Surveillance TipsПодробнее
Post-market surveillance as a medical device requirement in the EUПодробнее
Interactive Q&A August 20, 2021: Post-market Surveillance Requirements for Medical DevicesПодробнее
Webinar: How to set up post-market surveillance for your medical deviceПодробнее
Post market surveillance of medical devicesПодробнее
FDA Post Market Surveillance RequirementsПодробнее
EU MDR Post Market SurveillanceПодробнее
Medical Device ReportingПодробнее
Post Market Surveillance requirements under the new European Medical Device RegulationsПодробнее
Ensuring Patient Safety via Post-Market Surveillance for IoMTПодробнее
III ICEHTMC - Medical Devices: Post Market Surveillance (Inspection of Medical Devices).Подробнее
Purpose of the post-market surveillance process for medical devicesПодробнее
Understanding Post-Market Surveillance (PMS) for Medical DevicesПодробнее
Post-Market Surveillance for Medical Devices & Combination ProductsПодробнее
