Medical Devices News & Regulatory Info

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Matthias Fink’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Matthias Fink’s Presentation

Celegence Admin2024-02-14T06:24:31+00:00December 17th, 2020|

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Celegence Admin2024-02-14T06:24:49+00:00December 10th, 2020|

Economic Operators & Conclusions – EUDAMED Database Webinar

Economic Operators & Conclusions – EUDAMED Database Webinar

Celegence Admin2024-02-14T06:30:36+00:00November 24th, 2020|

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

Celegence2024-02-14T06:27:06+00:00November 17th, 2020|

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

Celegence Admin2024-02-14T06:27:17+00:00November 10th, 2020|

How to Start Preparing Your RA QA Team for The EUDAMED Database – Webinar Overview

How to Start Preparing Your RA QA Team for The EUDAMED Database – Webinar Overview

Celegence2024-02-14T06:27:25+00:00November 4th, 2020|

MDR Article 117: A New Implication for Drug-device Combination Products

MDR Article 117: A New Implication for Drug-device Combination Products

Celegence2021-05-11T07:08:38+00:00October 30th, 2020|

Implications of MDR for Medical Devices Incorporating Artificial Intelligence and Machine Learning

Implications of MDR for Medical Devices Incorporating Artificial Intelligence and Machine Learning

Celegence Admin2021-05-11T07:47:14+00:00October 27th, 2020|

RAPS Webinar Transcript – Q&A – Taking Advantage of the EU MDR Delay

RAPS Webinar Transcript – Q&A – Taking Advantage of the EU MDR Delay

Celegence Admin2024-02-14T06:27:44+00:00October 14th, 2020|

RAPS Webinar Transcript – Virtual Audits Q&A

RAPS Webinar Transcript – Virtual Audits Q&A

Celegence Admin2024-02-14T06:28:01+00:00October 12th, 2020|

Medical Device Blog

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Matthias Fink’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Matthias Fink’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Clinical Evaluations for Unique Product Types Under the EU MDR – Dr. Pratibha Mishra’s Presentation

Economic Operators & Conclusions – EUDAMED Database Webinar

Economic Operators & Conclusions – EUDAMED Database Webinar

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

SaMD, Brexit & Market Surveillance – EUDAMED Database Webinar

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

UDI & Product Types of Immediate Concern – EUDAMED Database Webinar

How to Start Preparing Your RA QA Team for The EUDAMED Database – Webinar Overview

How to Start Preparing Your RA QA Team for The EUDAMED Database – Webinar Overview

MDR Article 117: A New Implication for Drug-device Combination Products

MDR Article 117: A New Implication for Drug-device Combination Products

Implications of MDR for Medical Devices Incorporating Artificial Intelligence and Machine Learning

Implications of MDR for Medical Devices Incorporating Artificial Intelligence and Machine Learning

RAPS Webinar Transcript – Q&A – Taking Advantage of the EU MDR Delay

RAPS Webinar Transcript – Q&A – Taking Advantage of the EU MDR Delay

RAPS Webinar Transcript – Virtual Audits Q&A

RAPS Webinar Transcript – Virtual Audits Q&A

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