Implications for Medtech Companies with FDA Rollout of the New QMSR to Replace Current QSR Implications for Medtech Companies with FDA Rollout of the New QMSR to Replace Current QSRCelegence2024-02-14T05:55:07+00:00October 17th, 2022|
Implementing and Maintaining PMS and Performance Evaluation under the IVDR – Webinar Implementing and Maintaining PMS and Performance Evaluation under the IVDR – WebinarCelegence2024-02-02T11:33:10+00:00August 30th, 2022|
Unveiling Impactful Methods to Strengthen Device Claims – Webinar Unveiling Impactful Methods to Strengthen Device Claims – WebinarCelegence Admin2022-06-23T17:01:19+00:00June 23rd, 2022|
Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Productivity Improvements for Cost-Effective CER Writing & Maintenance – WebinarCelegence Admin2022-03-08T16:55:45+00:00March 8th, 2022|
Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices Webinar Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices WebinarCelegence Admin2022-02-14T12:53:27+00:00February 8th, 2022|
Ensuring Compliance For Your IVD’s Performance Evaluation – Webinar Ensuring Compliance For Your IVD’s Performance Evaluation – WebinarCelegence2022-07-01T05:58:31+00:00October 12th, 2021|
Process and Technology Innovation in EU MDR Compliance – Webinar Process and Technology Innovation in EU MDR Compliance – WebinarCelegence2023-01-17T05:24:21+00:00August 30th, 2021|
The Ins and Outs of Post Market Surveillance Under the EU MDR The Ins and Outs of Post Market Surveillance Under the EU MDRCelegence2024-04-24T16:27:32+00:00June 21st, 2021|
Medical Device Virtual Summit – Afternoon Program Medical Device Virtual Summit – Afternoon ProgramCelegence2024-02-14T06:21:53+00:00April 28th, 2021|
Medical Device Virtual Summit – Morning Program Medical Device Virtual Summit – Morning ProgramCelegence2024-02-14T06:21:25+00:00April 28th, 2021|