Medical Devices News & Regulatory Info

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|

Periodic Safety Update Reports (PSUR) Under the EU MDR 2017/745

Periodic Safety Update Reports (PSUR) Under the EU MDR 2017/745

Celegence Admin2022-02-23T13:39:01+00:00February 1st, 2022|

Cytotoxicity, Sensitization & Irritation Testing – Webinar w/ Thor Rollins Pt.2

Cytotoxicity, Sensitization & Irritation Testing – Webinar w/ Thor Rollins Pt.2

Celegence Admin2024-02-14T06:07:49+00:00January 25th, 2022|

Deep Dive: CAPTIS – MDR & IVDR Compliance Technology

Deep Dive: CAPTIS – MDR & IVDR Compliance Technology

Celegence Admin2022-06-22T14:26:00+00:00January 18th, 2022|

Progressive Roll-out of the In Vitro Diagnostics Medical Device Regulation in Europe (EU IVDR)

Progressive Roll-out of the In Vitro Diagnostics Medical Device Regulation in Europe (EU IVDR)

Celegence2022-02-23T13:40:58+00:00January 11th, 2022|

Cytotoxicity, Sensitization & Irritation Testing – The Big Three – Webinar w/ Thor Rollins

Cytotoxicity, Sensitization & Irritation Testing – The Big Three – Webinar w/ Thor Rollins

Celegence Admin2024-02-14T06:08:59+00:00December 15th, 2021|

Post Market Surveillance Under the EU MDR – Webinar Transcript – Q&A

Post Market Surveillance Under the EU MDR – Webinar Transcript – Q&A

Celegence2024-02-14T06:09:04+00:00December 8th, 2021|

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 2

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 2

Celegence2024-02-14T06:09:14+00:00November 30th, 2021|

Medical Device Blog

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

Periodic Safety Update Reports (PSUR) Under the EU MDR 2017/745

Periodic Safety Update Reports (PSUR) Under the EU MDR 2017/745

Cytotoxicity, Sensitization & Irritation Testing – Webinar w/ Thor Rollins Pt.2

Cytotoxicity, Sensitization & Irritation Testing – Webinar w/ Thor Rollins Pt.2

Deep Dive: CAPTIS – MDR & IVDR Compliance Technology

Deep Dive: CAPTIS – MDR & IVDR Compliance Technology

Progressive Roll-out of the In Vitro Diagnostics Medical Device Regulation in Europe (EU IVDR)

Progressive Roll-out of the In Vitro Diagnostics Medical Device Regulation in Europe (EU IVDR)

Cytotoxicity, Sensitization & Irritation Testing – The Big Three – Webinar w/ Thor Rollins

Cytotoxicity, Sensitization & Irritation Testing – The Big Three – Webinar w/ Thor Rollins

Post Market Surveillance Under the EU MDR – Webinar Transcript – Q&A

Post Market Surveillance Under the EU MDR – Webinar Transcript – Q&A

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 2

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 2

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