Medical Devices News & Regulatory Info

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|

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 1

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 1

Celegence Admin2024-02-14T06:09:40+00:00November 23rd, 2021|

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Q&A

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Q&A

Celegence2024-02-14T06:11:03+00:00November 2nd, 2021|

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 2

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 2

Celegence Admin2024-02-14T06:14:23+00:00October 28th, 2021|

Notified Bodies Under EU IVDR

Notified Bodies Under EU IVDR

Celegence Admin2022-02-23T13:37:08+00:00October 19th, 2021|

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 1

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 1

Celegence2024-02-14T06:14:10+00:00October 5th, 2021|

Medical Device Blog

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

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 1

Post Market Surveillance Under the EU MDR – Webinar Transcript – Part 1

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Q&A

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Q&A

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 2

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 2

Notified Bodies Under EU IVDR

Notified Bodies Under EU IVDR

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 1

Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 – Webinar Transcript Part 1

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