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.
MoreJapan's Adverse Event Glossary are amended to match with the IMDRF's terminologies.
MoreThe 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.
MoreOn September 17th, IMDRF, the International Medical Device Regulators Forum, has passed the proposal of Medical Device Clinical Evaluation, with unanimous approval of the IMDRF members. This proposal is written by Medical Device Clinical Evaluation Working Group, which is led by China NMPA.
MoreInternational Medical Device Regulators Forum (IMDRF) held a meeting in China during March 20 to 22. The current chairman, China FDA, proposed two projects and get the support from all IMDRF members.
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