泰國:公共衛生部宣布修訂醫療器材申請表 – 2020年3月
- 2020-03-16 07:03:45
公共衛生部關於根據部級條例修改申請表的公告,具體規定了《 2019年企業進口許可證》(第3號)和《 2019年企業製造許可證》註冊的規則,程序和條件。
了解更多公共衛生部關於根據部級條例修改申請表的公告,具體規定了《 2019年企業進口許可證》(第3號)和《 2019年企業製造許可證》註冊的規則,程序和條件。
了解更多泰國食品藥品監督管理局已經果斷地發布了公共衛生部公告,關於2019年將含酒精作為衛生用途的清潔產品,以及公共衛生部公告了2019年將含酒精的清潔產品在衛生用途。
了解更多Medical Devices (Amendment) Rules, 2020 has been newly issued to amend the Medical Devices Rules, 2017. Medical Devices (Amendment) Rules, 2020 will be effective 1st April 2020. All medical devices in India is now to be regulated as “drugs”.
了解更多Medical Devices (Amendment) Rules, 2020 has been newly issued to amend the Medical Devices Rules, 2017, effective 1st April 2020. All medical devices in India is now to be regulated as “drugs”.
了解更多It is Qualtech priority to deliver the most update and accurate news to our clients as well as performing as platform to all associated organization. OMETA is one of the organizations that has a lengthy association with Qualtech Corporation.
了解更多醫療器械部門將繼續進行試驗,以研究對當地負責人(LRP)的可行性,該試驗將持續到2020年12月31日,以用於有限數量的II / III / IV級普通醫療器械的上市申請。
了解更多Ministry of Health has issued a Circular letter number HK.02.02 / VI / 1465/2019 about withdrawal and elimination of medical devices that contain mercury from the market. This circular letter is addressed to Head of medical devices manufacturer and Head of medical device distributor in throughout Indonesia. They need to take several actions to help the withdrawal and elimination process of medical devices that contain mercury.
了解更多根據印度尼西亞衛生部的適用法規,醫療器械必須經過印度尼西亞衛生部的評估過程,才能獲得銷售授權號。 該銷售授權號表示醫療設備已經過
了解更多VN MOH發布了第03/2020號法令,以修訂第36和169號法令,該法令將於2020年1月1日生效。以下是與進口醫療設備有關的說明:經與第36和169號法令相比,Qualtech進行差異性說明。
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