• 2020-02-21 07:20:48

The Ministry of Health (MoH) was recently notified by the MDA on a 'headphone' device that allegedly reduces and controls blood sugar levels, published through a local newspaper.

• 2020-02-21 07:19:49

CDSCO India has issued an extension for several types of medical devices to register for market authorization, some until January 2021 while the other types have until April 2021.

• 2020-02-21 07:19:00

Eight notified bodies have now been registered with the CDSCO intends to carry out audit of a manufacturing site of Class A or Class B of medical devices.

• 2020-02-21 07:17:09

HSA released a draft guidance for software regulation last December 2019. The draft includes detailed explanation of regulation from pre-marketing approval to post market monitoring of software devices. The Singaporean authority would like to ask for stakeholder comments before official implementation

• 2020-02-15 09:11:10

Friendly interface and specific information could make you much more easily to know Qualtech and latest regulatory around the Asian countries.

• 2020-02-15 08:22:55

In order to provide customers with more complete medical device regulatory services in the Asian region, Qualtech establishs service presence in Malaysia.

• 2020-02-21 07:16:25

In order to maintain the safety and efficacy of a medical device, a surveillance system is needed. Therefore, medical device distributors in Indonesia are recommended to comply with CDAKB / Good Distribution Practice of Medical Device.

• 2020-02-21 07:15:43

As implemented starting from July 9th 2018, the Indonesian Government keeps developing the OSS system to actualize the acceleration of licensing process in Indonesia.

• 2020-02-21 07:14:51

Health spending is growing faster than the overall economy globally as well as in most countries. In this article, we are looking at the healthcare expenditure and medical device demand trends in China, Thailand, Malaysia and Singapore, to understand how their government are spending to improve the living standard of their citizens.

• 2020-02-21 07:12:37

On December 20, 2019, the NMPA issued an update of the Exemption List from Clinical Trials in China for Medical Device (hereinafter simply referred to as the “Exemption list"), which includes "medical devices" and "in vitro diagnostic devices".