Medical Devices News & Regulatory Info

Enhancing Post-Market Surveillance: Strengthening Medical Device Regulation in the UK

Enhancing Post-Market Surveillance: Strengthening Medical Device Regulation in the UK

Celegence2023-09-26T15:42:52+00:00August 8th, 2023|

UDI Requirements for Contact Lens Manufacturers – European Commission Amendments

UDI Requirements for Contact Lens Manufacturers – European Commission Amendments

Celegence2023-09-27T12:40:28+00:00August 8th, 2023|

Strategies for Successful CE Certification: Mitigating Non-Conformities and Streamlining Review Cycles

Strategies for Successful CE Certification: Mitigating Non-Conformities and Streamlining Review Cycles

Celegence2024-04-24T15:39:05+00:00May 26th, 2023|

Clinical Benefits and Equivalence: A Comprehensive Guide to EU MDR Clinical Evaluation

Clinical Benefits and Equivalence: A Comprehensive Guide to EU MDR Clinical Evaluation

Celegence2024-04-25T12:07:57+00:00May 26th, 2023|

Extending MDR/IVDR Transitional Period and Eliminating ‘Sell-Off’ Periods – (EU) 2023/607

Extending MDR/IVDR Transitional Period and Eliminating ‘Sell-Off’ Periods – (EU) 2023/607

Celegence2023-07-11T12:20:45+00:00May 26th, 2023|

Europe PMC Integration – CAPTIS™ Features

Europe PMC Integration – CAPTIS™ Features

Celegence2023-03-17T11:07:12+00:00March 16th, 2023|

CAPTIS™ Time Saving Study

CAPTIS™ Time Saving Study

Celegence2023-10-02T10:50:48+00:00March 6th, 2023|

Data Extraction Tables – CAPTIS™ Feature

Data Extraction Tables – CAPTIS™ Feature

Celegence2023-01-27T18:35:14+00:00January 27th, 2023|

Automatic Literature Report Generation – CAPTIS™ Feature

Automatic Literature Report Generation – CAPTIS™ Feature

Celegence2023-01-13T11:34:57+00:00January 13th, 2023|

FDA MAUDE / TPLC Integration – CAPTIS™ Feature

FDA MAUDE / TPLC Integration – CAPTIS™ Feature

Celegence2022-12-02T09:25:06+00:00December 1st, 2022|

Medical Device Blog

Enhancing Post-Market Surveillance: Strengthening Medical Device Regulation in the UK

Enhancing Post-Market Surveillance: Strengthening Medical Device Regulation in the UK

UDI Requirements for Contact Lens Manufacturers – European Commission Amendments

UDI Requirements for Contact Lens Manufacturers – European Commission Amendments

Strategies for Successful CE Certification: Mitigating Non-Conformities and Streamlining Review Cycles

Strategies for Successful CE Certification: Mitigating Non-Conformities and Streamlining Review Cycles

Clinical Benefits and Equivalence: A Comprehensive Guide to EU MDR Clinical Evaluation

Clinical Benefits and Equivalence: A Comprehensive Guide to EU MDR Clinical Evaluation

Extending MDR/IVDR Transitional Period and Eliminating ‘Sell-Off’ Periods – (EU) 2023/607

Extending MDR/IVDR Transitional Period and Eliminating ‘Sell-Off’ Periods – (EU) 2023/607

Europe PMC Integration – CAPTIS™ Features

Europe PMC Integration – CAPTIS™ Features

CAPTIS™ Time Saving Study

CAPTIS™ Time Saving Study

Data Extraction Tables – CAPTIS™ Feature

Data Extraction Tables – CAPTIS™ Feature

Automatic Literature Report Generation – CAPTIS™ Feature

Automatic Literature Report Generation – CAPTIS™ Feature

FDA MAUDE / TPLC Integration – CAPTIS™ Feature

FDA MAUDE / TPLC Integration – CAPTIS™ Feature

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