Medical Devices News & Regulatory Info

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|

Guidance on Addressing Cybersecurity of Connected Medical Devices

Guidance on Addressing Cybersecurity of Connected Medical Devices

Celegence Admin2021-05-11T07:58:43+00:00July 16th, 2020|

Medical Device Labeling Changes and Challenges Under EU MDR

Medical Device Labeling Changes and Challenges Under EU MDR

Celegence Admin2021-05-11T06:34:38+00:00July 6th, 2020|

Components of an Effective Post-Market Surveillance for Medical Devices

Components of an Effective Post-Market Surveillance for Medical Devices

Celegence Admin2021-05-11T08:07:15+00:00July 2nd, 2020|

Remote Medical Audits During COVID-19

Remote Medical Audits During COVID-19

Celegence2021-05-11T08:20:58+00:00June 2nd, 2020|

Addressing the Regulatory Challenges with Software as a Medical Device in EU MDR

Addressing the Regulatory Challenges with Software as a Medical Device in EU MDR

Celegence Admin2021-05-11T08:27:44+00:00May 14th, 2020|

Medical Device Blog

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

Guidance on Addressing Cybersecurity of Connected Medical Devices

Guidance on Addressing Cybersecurity of Connected Medical Devices

Medical Device Labeling Changes and Challenges Under EU MDR

Medical Device Labeling Changes and Challenges Under EU MDR

Components of an Effective Post-Market Surveillance for Medical Devices

Components of an Effective Post-Market Surveillance for Medical Devices

Remote Medical Audits During COVID-19

Remote Medical Audits During COVID-19

Addressing the Regulatory Challenges with Software as a Medical Device in EU MDR

Addressing the Regulatory Challenges with Software as a Medical Device in EU MDR

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