• 2020-02-14 04:08:31

Outcomes of these consultation sessions have been consolidated and new revisions to the existing guidance documents and issuance of new guidance documents are to be carried out in stages, after this.

• 2020-02-14 04:06:17

Vietnam Ministry of Health released the draft decree mention some points of Medical Device Management under Decree 36/2016/ND-CP. After the detailed analysis, Qualtech has outlined five major differences between the new and previous version of regulations:

• 2020-02-14 04:05:14

This month’s updates include the "Internet+Medical Health", “the Special Approval Procedure for Innovative Medical Devices”, “the Revision Plan of Medical Device Standards” among others. All information you need to know has been put in a nutshell:

• 2020-02-14 04:04:20

Administrative Order 2018-117, otherwise known as the “Effectivity of the New Schedule of Fees” was released in the 2nd of April, 2018 to inform all the FDA Stakeholders and the General Public that a new schedule of fees shall be implemented on the 30th of June 2018.

• 2020-02-12 16:02:17

Health Sciences Authority (HSA) published the list of new fees applicable to health products including Medical devices, on last August 1, 2018.

• 2020-08-06 09:09:52

• 2020-02-14 07:33:20

In order to support the development of medical devices urgently needed for clinical purposes (hereinafter referred to as "emergency devices"), such as “for life-threatening cases, or diseases that may endanger public health, CMDE has released a draft of the basic principles of medical devices urgently needed in clinical purposes that may be conditionally approved to accelerate medical device listing.

• 2020-02-14 07:32:41

The Council decides to suspend the implementation of Clause 11 of the Medical Device Registration and Management in the Hainan tourism area. In order to support this suspension, CNDA has released a temporary Order, entitled “The Supervision Regulation of Emergency Medical Devices in Hainan International Tourism Area”. The scope of this Order includes all medical devices that are urgently needed for clinical purposes, operation conditions, and a

• 2020-02-14 07:32:02

The new medical device rule “MDR 2017, India” has come into effect from January 2018. In line with that, the CDSCO (Central Drug Standard Control Organization) has recently been releasing guidance documents,

• 2020-02-14 07:29:47

Medical Device Authority (MDA), Malaysia has recently introduced a new initiative calling for e-mail notification subscription by all interested stakeholders. This new initiative by MDA aims to provide the latest information to stakeholders and general public who wish to subscribe to this service,