• 2020-02-12 15:04:32

In Medical Device Act 2012 (Act 737) of Malaysia, there is no specific provision for medical devices imported/exported from/to countries without diplomatic ties with Malaysia, such as Israel. Malaysia has not acknowledged Israel as an independent sovereign state.

• 2020-02-12 15:03:41

In Malaysia, medical devices procurement by local healthcare institutions are heavily controlled in order to make sure the supplied medical devices are safe and efficient. For starters, there are many procurement methods, depending on the product’s market value.

• 2020-02-12 15:01:28

In order to effectively inform the stakeholders of these new regulations, HSA Medical Branch published the updated documents containing the overview of the whole Singapore regulation unto their website.

• 2020-02-12 15:00:06

Slight revision on guidance documents about Singapore Standards and Medical devices for exhibition were added last July 2018.

• 2020-02-12 14:58:58

In order to unify the management of medical device import license, MoH informed and stopped receiving the contents of request for adjustment of import license which has a validity period until Dec 31st, 2017 granted in accordance to Circular No. 30/2015/TT-BYT.

• 2020-02-12 14:56:43

This month’s updates include the "Medical Devices Procurement for Healthcare Institutions ", “Announcement Regarding Registration Application of Medical Devices and Licensed Establishment”, “Exemption from Registration Requirement for Export Only Medical Device” among others. All information you need to know have been summed up in a nutshell.

• 2020-02-13 06:02:57

It has been earlier established that Medical Device Authority (MDA) and National Pharmaceutical Regulatory Agency (NPRA) of Malaysia will start to regulate drug-medical device and medical device-drug combination products together, starting July 1st, 2019.

• 2020-02-13 05:57:27

The Medical Device Authority (MDA) has been set on stricter implementing and enforcing the Medical Device Act 2012 (Act 737) via the gradual introduction of various policies. In 2016, it issued a policy providing a transition period of two (2) years for all local and foreign manufacturers importing,

• 2020-02-12 16:00:39

The list of medical equipment defined with HS codes issued together with this Circular is the basis for organizations and individuals to make customs declarations when exporting or importing medical equipment into Vietnam.

• 2020-02-14 04:03:25

海外医機器技術協力会(OMETA), Japan Association of Medical Device Industry (JAMDI), DEKRA Japan, and Qualtech Japan are jointly organising an upcoming seminar in early July (July 6th, 2018) in Japan.