Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

Clinical Evaluation of Medical Devices according to EU MDR 2017 745Подробнее

Clinical Evaluation of Medical Devices according to EU MDR 2017 745

The New EU MDR PMS Requirements WebinarПодробнее

The New EU MDR PMS Requirements Webinar

EU Medical Device Regulation WebinarПодробнее

EU Medical Device Regulation Webinar

Best Practices to Write a EU MDR Clinical Evaluation Report (CER) - A Webinar Video SARACASolutionsПодробнее

Best Practices to Write a EU MDR Clinical Evaluation Report (CER) - A Webinar Video SARACASolutions

The Road to Market Authorization for Sterile Medical Devices within the EUПодробнее

The Road to Market Authorization for Sterile Medical Devices within the EU

A Year of EU MDR Remediation: Biocompatibility Strategies and Lessons LearnedПодробнее

A Year of EU MDR Remediation: Biocompatibility Strategies and Lessons Learned

Clinical Evidence for Medical Devices Under Regulation (EU) 2017/745Подробнее

Clinical Evidence for Medical Devices Under Regulation (EU) 2017/745

What is clinical evaluation under MDR ?Подробнее

What is clinical evaluation under MDR ?

Webinar: Clinical Investigations - Transitioning from MDD to MDRПодробнее

Webinar: Clinical Investigations - Transitioning from MDD to MDR

All about PMCF with Cesare Magri [EU MDR 2017/745]Подробнее

All about PMCF with Cesare Magri [EU MDR 2017/745]

MDR Effects on Medical Device ProcessingПодробнее

MDR Effects on Medical Device Processing

Short course on the Medical Device Regulation (EU) 2017/745Подробнее

Short course on the Medical Device Regulation (EU) 2017/745

RAPS Sponsored Webinar: Understanding Key Components of a Clinical EvaluationПодробнее

RAPS Sponsored Webinar: Understanding Key Components of a Clinical Evaluation

Clinical/Performance evaluation for Medical Device Software (MDR IVDR)Подробнее

Clinical/Performance evaluation for Medical Device Software (MDR IVDR)

Current Challenges in MDR (Medical Device Regulation) in the EU - Webinar with NO-FEAR ProjectПодробнее

Current Challenges in MDR (Medical Device Regulation) in the EU - Webinar with NO-FEAR Project

EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745Подробнее

EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745

Combination Products: Seeking Notified Body Opinion According to Article 117 - WebinarПодробнее

Combination Products: Seeking Notified Body Opinion According to Article 117 - Webinar

Medical Device Regulations (MDR) Webinar | Recorded by BES Chairman Dirk ter HaarПодробнее

Medical Device Regulations (MDR) Webinar | Recorded by BES Chairman Dirk ter Haar

The Ins and Outs of PMS Requirements Under the EU MDR - WebinarПодробнее

The Ins and Outs of PMS Requirements Under the EU MDR - Webinar

Webinar | Safer medical devices: Implementation of the EU MDR and EUDAMED databaseПодробнее

Webinar | Safer medical devices: Implementation of the EU MDR and EUDAMED database