Medical Devices News & Regulatory Info

Introducing CAPTIS Copilot – An AI Assistant Purposefully Built for the Life Science Industry

Introducing CAPTIS Copilot – An AI Assistant Purposefully Built for the Life Science Industry

Celegence2023-10-04T16:32:16+00:00October 4th, 2023|

Systematic Literature Review Tools – What To Look For When Choosing One

Systematic Literature Review Tools – What To Look For When Choosing One

Celegence2023-09-13T11:40:03+00:00September 13th, 2023|

510k Submission Planning – Expert Tips for Medical Device Manufacturers

510k Submission Planning – Expert Tips for Medical Device Manufacturers

Celegence Admin2023-08-22T15:39:23+00:00August 22nd, 2023|

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|

Medical Device Blog

Introducing CAPTIS Copilot – An AI Assistant Purposefully Built for the Life Science Industry

Introducing CAPTIS Copilot – An AI Assistant Purposefully Built for the Life Science Industry

Systematic Literature Review Tools – What To Look For When Choosing One

Systematic Literature Review Tools – What To Look For When Choosing One

510k Submission Planning – Expert Tips for Medical Device Manufacturers

510k Submission Planning – Expert Tips for Medical Device Manufacturers

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

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