주문형 웹 세미나

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Optimization for Global Vigilance Reporting

In this on-demand webinar, our Emergo by UL subject matter expert shares insights on optimization for global vigilance reporting.

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Open Forum: Use-Related Risk Analysis Q&A

During this interactive session, our senior HFE experts answer pre-submitted and live questions about conducting and documenting use-related risk analyses of medical devices.

Regulation (EU) 2024/1860 and IVDR Compliance in Europe

In this on-demand webinar, our Emergo by UL subject matter expert will share insights on Regulation (EU) 2024/1860 and IVDR transition periods in Europe.

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Risk Analysis for Design and Innovation

Consider use-related risk analysis in simple terms, so that you can start early and use it as a powerful tool for creative output.

Importer/Distributor MDR Requirements and Impacts for Manufacturers

In this on-demand webinar, our Emergo by UL expert shares insights on importer/distributor MDR requirements and impacts for manufacturers.

Open Forum: Human Factors Usability Testing Q&A

During this interactive session, our senior HFE experts answered pre-submitted and live questions about conducting usability testing of medical devices.

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Japan Regulatory Requirements – Medical Device Software

In this on-demand webinar, our Emergo by UL subject matter expert shares insights on Japanese regulatory requirements for medical device software.

Optimizing a QMS for Medical Device Companies

In this on-demand webinar, our Emergo by UL subject matter expert shares insights on how to optimize a QMS for global medical device companies.

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Best Practices for Engaging with the US FDA on Human Factors Strategy

Learn how to effectively prepare for and engage with the U.S. FDA via pre-submissions and live meetings focused on a wide range of HFE topics.

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Medical Device Software and Cybersecurity

Maintaining safer medical devices: how medical device regulations, standards and guidance are keeping pace with the proliferation of medical device software.

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Conducting a Comparative Analysis in Lieu of HF Validation Testing

Learn how to conduct effective comparative analysis as an alternative approach to HF validation testing.

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Revised IVD Regulation RDC 830/2023

In this on-demand webinar, our Emergo by UL subject matter expert shares insights on how to navigate revised IVD regulation RDC 830/2023.

주문형 웹 세미나

저희는 저희 일에 관해 이야기하는 것을 좋아합니다. 라이브 웨비나, 워크숍, 무역 박람회를 통해 이머고 전문가들이 제공하는 정보를 획득하세요.

필터링 기준

Optimization for Global Vigilance Reporting

Open Forum: Use-Related Risk Analysis Q&A

Regulation (EU) 2024/1860 and IVDR Compliance in Europe

Risk Analysis for Design and Innovation

Importer/Distributor MDR Requirements and Impacts for Manufacturers

Open Forum: Human Factors Usability Testing Q&A

Japan Regulatory Requirements – Medical Device Software

Optimizing a QMS for Medical Device Companies

Best Practices for Engaging with the US FDA on Human Factors Strategy

Medical Device Software and Cybersecurity

Conducting a Comparative Analysis in Lieu of HF Validation Testing

Revised IVD Regulation RDC 830/2023

전문가에게 자세한 정보 요청

감사합니다! 요청이 접수되었습니다.

주문형 웹 세미나

저희는 저희 일에 관해 이야기하는 것을 좋아합니다. 라이브 웨비나, 워크숍, 무역 박람회를 통해 이머고 전문가들이 제공하는 정보를 획득하세요.

필터링 기준 Loading...

필터링 기준

Optimization for Global Vigilance Reporting

Open Forum: Use-Related Risk Analysis Q&A

Regulation (EU) 2024/1860 and IVDR Compliance in Europe

Risk Analysis for Design and Innovation

Importer/Distributor MDR Requirements and Impacts for Manufacturers

Open Forum: Human Factors Usability Testing Q&A

Japan Regulatory Requirements – Medical Device Software

Optimizing a QMS for Medical Device Companies

Best Practices for Engaging with the US FDA on Human Factors Strategy

Medical Device Software and Cybersecurity

Conducting a Comparative Analysis in Lieu of HF Validation Testing

Revised IVD Regulation RDC 830/2023

전문가에게 자세한 정보 요청

감사합니다! 요청이 접수되었습니다.