JAPAN: Adverse Event Glossary are Amended to Match with the Amended IMDRF's Terminologies - May, 2022
- 2022-05-26 13:46:04
Japan's Adverse Event Glossary are amended to match with the IMDRF's terminologies.
了解更多
Japan's Adverse Event Glossary are amended to match with the IMDRF's terminologies.
了解更多
The Japan Federation of Medical Devices Association (JFMDA) has arranged the Japanese “Adverse Event Glossary” and created a mapping chart to match with IMDRF's Adverse Event terminologies.
了解更多
In July, MOH released two Official Dispatches as guidance on registration routes and document preparation to import SARS-CoV-2 IVD medical devices and biologicals, especially SASR-CoV-2 Antigen Rapid Test Kit (RTK).
了解更多
Health Sciences Authority (HSA) launched Pandemic Special Access Route (PSAR) for important therapeutic products essential for pandemic response. HSA defined the group of products that can apply via this route and the requirements/criteria for submission.
了解更多我們透過Cookies蒐集您的瀏覽記錄,以了解您如何使用我們的網站,從而分析及改善您的體驗。如繼續使用我們的網站,即表示您接受我們使用 Cookies。