Medical Devices News & Regulatory Info

Medical Device UDI Requirements in the US and Europe

Medical Device UDI Requirements in the US and Europe

Celegence2024-04-25T11:08:35+00:00July 4th, 2022|

PRISMA Flow Diagram – CAPTIS™ Features

PRISMA Flow Diagram – CAPTIS™ Features

Celegence2022-06-22T14:25:59+00:00June 9th, 2022|

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 2

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 2

Celegence2024-02-14T06:03:17+00:00May 19th, 2022|

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 1

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 1

Celegence2024-02-14T06:03:24+00:00May 13th, 2022|

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Q&A

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Q&A

Celegence Admin2024-02-14T06:05:18+00:00April 19th, 2022|

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Transcript

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Transcript

Celegence2024-02-14T06:05:31+00:00April 13th, 2022|

Clinical Performance Under IVDR

Clinical Performance Under IVDR

Celegence2022-10-17T13:46:32+00:00April 6th, 2022|

Systematic Literature Reviews Made Easy – Why You Should Switch to CAPTIS™

Systematic Literature Reviews Made Easy – Why You Should Switch to CAPTIS™

Celegence2022-10-17T13:45:05+00:00March 29th, 2022|

The Role of Harmonized Standards for Compliance to MDR and IVDR

The Role of Harmonized Standards for Compliance to MDR and IVDR

Celegence2022-03-01T17:38:52+00:00March 1st, 2022|

How to Choose the Right Conformity Assessment Route for CE Marking your IVD Product

How to Choose the Right Conformity Assessment Route for CE Marking your IVD Product

Celegence2022-02-23T14:26:38+00:00February 22nd, 2022|

Medical Device Blog

Medical Device UDI Requirements in the US and Europe

Medical Device UDI Requirements in the US and Europe

PRISMA Flow Diagram – CAPTIS™ Features

PRISMA Flow Diagram – CAPTIS™ Features

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 2

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 2

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 1

Ensuring Compliance for your IVD’s Performance Evaluation – Webinar Transcript – Part 1

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Q&A

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Q&A

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Transcript

Productivity Improvements for Cost-Effective CER Writing & Maintenance – Webinar Transcript

Clinical Performance Under IVDR

Clinical Performance Under IVDR

Systematic Literature Reviews Made Easy – Why You Should Switch to CAPTIS™

Systematic Literature Reviews Made Easy – Why You Should Switch to CAPTIS™

The Role of Harmonized Standards for Compliance to MDR and IVDR

The Role of Harmonized Standards for Compliance to MDR and IVDR

How to Choose the Right Conformity Assessment Route for CE Marking your IVD Product

How to Choose the Right Conformity Assessment Route for CE Marking your IVD Product

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