オンデマンドウェビナー

Group of business professionals having a meeting while looking at a map of the world

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.

Scientist woman lab technical service observe liquid sample with lab glassware and test tubes in chemical laboratory

日米欧におけるIVDの規制要件と最新情報

日米欧の体外診断用医薬品/体外診断用医療機器（IVD）に関する規制の概要および最新情報を弊社コンサルタントが日本語で解説いたします。

Group of people raising their hands to ask questions

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.

Three coworkers collaborating together in front of a whiteboard covered in post-it notes

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.

Three coworkers collaborating together in front of a tablet

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.

Three business colleagues reviewing metrics in a meeting

QMS外部監査に向けた準備

ISO認証機関、MDSAP監査組織、FDAなどによるQMS外部監査に向けた最適な準備について解説いたします。

Group of business professionals having a discussion while looking at a tablet on a table

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.

Group of colleagues having a meeting in a contemporary office setting

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.

オンデマンドウェビナー

当社の活動について喜んでお話しします。ライブのウェビナー、ワークショップ、展示会を通じて、当社の専門家から知識を得てください。

次の条件で絞り込み

Optimization for Global Vigilance Reporting

日米欧におけるIVDの規制要件と最新情報

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

QMS外部監査に向けた準備

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

Medical Device Software and Cybersecurity

弊社専門スタッフにお問い合わせください。

ありがとうございました。

オンデマンドウェビナー

当社の活動について喜んでお話しします。 ライブのウェビナー、ワークショップ、展示会を通じて、当社の専門家から知識を得てください。

次の条件で絞り込み Loading...

次の条件で絞り込み

Optimization for Global Vigilance Reporting

日米欧におけるIVDの規制要件と最新情報

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

QMS外部監査に向けた準備

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

Medical Device Software and Cybersecurity

弊社専門スタッフにお問い合わせください。

ありがとうございました。

当社の活動について喜んでお話しします。ライブのウェビナー、ワークショップ、展示会を通じて、当社の専門家から知識を得てください。