Medical Devices News & Regulatory Info

Medical Device Approvals – FDA Vs EU MDR

Medical Device Approvals – FDA Vs EU MDR

Celegence2022-02-23T13:36:28+00:00March 10th, 2021|

Approach to Authoring a Clinical Evaluation Report Under the EU MDR

Approach to Authoring a Clinical Evaluation Report Under the EU MDR

Celegence Admin2022-02-23T13:27:13+00:00February 25th, 2021|

Clinical Evaluation Report – Introduction to Clinical Reports

Clinical Evaluation Report – Introduction to Clinical Reports

Celegence2021-05-11T07:25:48+00:00February 3rd, 2021|

Why Software as a Medical Device (SaMD) is Prioritized in the EU MDR – Industry Perspective

Why Software as a Medical Device (SaMD) is Prioritized in the EU MDR – Industry Perspective

Celegence Admin2021-09-16T18:04:22+00:00January 12th, 2021|

Clinical Evaluations for Unique Product Types Under the EU MDR – Q&A

Clinical Evaluations for Unique Product Types Under the EU MDR – Q&A

Celegence Admin2024-02-14T06:24:11+00:00January 4th, 2021|

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|

Medical Device Blog

Medical Device Approvals – FDA Vs EU MDR

Medical Device Approvals – FDA Vs EU MDR

Approach to Authoring a Clinical Evaluation Report Under the EU MDR

Approach to Authoring a Clinical Evaluation Report Under the EU MDR

Clinical Evaluation Report – Introduction to Clinical Reports

Clinical Evaluation Report – Introduction to Clinical Reports

Why Software as a Medical Device (SaMD) is Prioritized in the EU MDR – Industry Perspective

Why Software as a Medical Device (SaMD) is Prioritized in the EU MDR – Industry Perspective

Clinical Evaluations for Unique Product Types Under the EU MDR – Q&A

Clinical Evaluations for Unique Product Types Under the EU MDR – Q&A

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

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