2013年7月30日在東京舉行的有關台灣和中國大陸監管註冊的演講 2013年7月
- 2020-02-15 08:52:37
Qualtech受OMEGA(海外醫療設備技術助理)的邀請在台灣和中國大陸進行法規註冊演講。
了解更多Qualtech受OMEGA(海外醫療設備技術助理)的邀請在台灣和中國大陸進行法規註冊演講。
了解更多2013年6月25日至6月26日,Qualtech TFDA經理張敏娜(Juliana Chang)應新加坡製造業聯合會和DH RegSys Pte Ltd的邀請在新加坡進行了TFDA培訓。
了解更多Every once in a while, Japanese Ministry of Health, Labor and Welfare (MHLW) issues notices to announce evaluation principles of “Next-Generation Medical Devices,” to accelerate review and approval process of new medical devices which has high demands and high feasibility of product realization. Since 2008, there have been 27 issuances by MHLW listed in the end of this article.
In this article, we will introduce list of “Next-Generation Medical Devices” that were announced in the past notices as well as were one of the notices issued in September of 2020, “Evaluation Index of Medical Devices for Home Medical Care”.
Every once in a while, Japanese Ministry of Health, Labor and Welfare (MHLW) issues notices to announce evaluation principles of “Next-Generation Medical Devices,” to accelerate review and approval process of new medical devices which has high demands and high feasibility of product realization. Since 2008, there have been 27 issuances by MHLW listed in the end of this article.
In this article, we will introduce list of “Next-Generation Medical Devices” that were announced in the past notices as well as were one of the notices issued in September of 2020, “Evaluation Index of Medical Devices for Home Medical Care”.
泰國公共衛生部宣布了一套醫療器械定義,供製造商和進口商根據基於風險的分類註冊其醫療器械時應遵循,以逐步支持泰國從基於政策的分類過渡。
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