• 2020-03-16 07:03:45

Ministry of Public Health Announcement regarding Amendment of the Application Form in accordance with the Ministerial Regulations, Specify the Rules, Procedures and Conditions for Registration of Establishment Import License 2019 (No.3) and Registration of Establishment Manufacturing License 2019.

• 2020-03-16 07:02:46

ThaiFDA has decisively made an announcement by Ministry of Public Health Announcement regarding Cleaning Products Containing Alcohol as a Component for Hygienic Use 2019 and Ministry of Public Health Announcement regarding Cleaning Products Containing Alcohol as a Component for Hygienic Use 2019.

• 2020-03-16 06:50:01

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”.

• 2020-03-16 06:48:29

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”.

• 2020-03-16 06:46:58

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.

• 2020-03-16 06:42:41

The Medical Device Division will continue the trial to study the feasibility for Local Responsible Persons (LRP),the trial will last until 31 December 2020 for a limited number of listing applications of Class II/III/IV general medical devices. 

• 2020-03-16 06:38:53

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.

• 2020-03-16 06:34:36

In accordance with applicable regulations of MOH Indonesia, medical devices must go through an assessment process by the MOH Indonesia to obtain a marketing authorization number. This marketing authorization number means that the medical devices have been declared safe and efficacy.

• 2020-03-16 06:31:12

In a latest announcement, MDA has announced that unregistered face masks shall henceforth be placed in the market via a Special Access route.

• 2020-02-21 07:28:40

VN MOH released the Decree 03/2020, to amend Decree 36 & 169, which is effective from Jan 1, 2020. Below are remarks relating to the imported Medical Device as below: Qualtech marks up the different place comparing to Decree 36 & 169.