Medical Devices News & Regulatory Info

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|

RAPS Webinar Transcript – MDR Non Conformance Q&A With Dr. Greg Shipp

RAPS Webinar Transcript – MDR Non Conformance Q&A With Dr. Greg Shipp

Celegence Admin2024-02-14T06:28:17+00:00October 7th, 2020|

RAPS Webinar Transcript – Dr Royth von Hahn’s Presentation on EU MDR Extension

RAPS Webinar Transcript – Dr Royth von Hahn’s Presentation on EU MDR Extension

Celegence Admin2024-02-14T06:28:38+00:00October 1st, 2020|

RAPS Webinar Transcript – Dr Vaillot’s Presentation on EU MDR Extension

RAPS Webinar Transcript – Dr Vaillot’s Presentation on EU MDR Extension

Celegence2024-02-14T06:28:45+00:00September 22nd, 2020|

Guidance on Identifying the Person Responsible for Regulatory Compliance under MDR and IVDR

Guidance on Identifying the Person Responsible for Regulatory Compliance under MDR and IVDR

Celegence Admin2021-05-11T07:52:07+00:00August 26th, 2020|

Risk Management Requirement Under MDR

Risk Management Requirement Under MDR

Celegence Admin2024-10-02T14:32:35+00:00July 30th, 2020|

Medical Device Blog

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

RAPS Webinar Transcript – MDR Non Conformance Q&A With Dr. Greg Shipp

RAPS Webinar Transcript – MDR Non Conformance Q&A With Dr. Greg Shipp

RAPS Webinar Transcript – Dr Royth von Hahn’s Presentation on EU MDR Extension

RAPS Webinar Transcript – Dr Royth von Hahn’s Presentation on EU MDR Extension

RAPS Webinar Transcript – Dr Vaillot’s Presentation on EU MDR Extension

RAPS Webinar Transcript – Dr Vaillot’s Presentation on EU MDR Extension

Guidance on Identifying the Person Responsible for Regulatory Compliance under MDR and IVDR

Guidance on Identifying the Person Responsible for Regulatory Compliance under MDR and IVDR

Risk Management Requirement Under MDR

Risk Management Requirement Under MDR

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