• 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 04:22:39

The ASEAN Medical Device Directive (AMDD) was signed by the ten (10) Member States in 2015, with the main objective of harmonizing the medical device regulations and common technical documents which may help medical manufacturers easily penetrate the ASEAN Medical Device Market.

• 2020-02-14 07:53:58

edtec Japan, Asia’s largest tradeshow dedicated to the design and manufacturing of medical devices will take place from 18 to 20 in April 2018 at Tokyo Big Sight. Qualtech, as a professional medical device regulatory consulting firm in Asia, will participate the event this year to provide regulatory solution for all medical devices to meet the requirement in Asia countries

• 2020-02-14 07:42:08

On 30th of November 2017, following recommendation from the Advisory Board, Thai FDA had announced four new checkpoints which regulate importation and exportation of medical devices. The new checkpoints are located in four different provinces as follows:

• 2020-02-14 07:47:54

The Guidelines released by the Department of Health concerning Medical Device Registration is in place to be officiated following its publication. This shall be implemented a year after its effective date. Delayed implementation allows sufficient preparation for applicants in securing technical documents crucial to the registration process.

• 2020-02-14 07:52:35

In an effort to showcase the latest developments in the medical, dental and pharmaceutical industry, the MEDICAL Philippines, in partnership with Pharma Philippines and Dental Philippines will be holding a Medical Expo which serves to bring international congregation of Medical & Healthcare equipment and services, Dental Technology,

• 2020-02-14 14:54:42

In order to enhance the inspection of imported drugs and medical devices, China Food and Drug Administration (CFDA) has issued “Draft of Regulations for The Administration of Overseas Inspection of Drug and Medical Devices”. It is currently looking for public comments until January 24, 2018.

• 2020-02-14 14:52:01

Starting from January 1, 2018, the Malaysian Communications and Multimedia Commission (MCMC) no longer permits any kind of Short Range Devices (SRD) and Radio Frequency Identification Devices (RFID) to operate in the frequency range from 869 MHz to 870 MHz.

• 2020-02-14 15:24:31

According to the post-show figures from the organizer, PT. OSI, indicate that medical device should be set for a prosperous year ahead in 2018 of a record-breaking attendance of more than 43,869 and 518 exhibitors from 46 countries. Around 40% of exhibitors were international, with more than 54% from China, 22% from Taiwan and 12% from South Korea.

• 2020-02-14 15:23:25

On November 14th 2017, Center for Medical Device Evaluation (CMDE) released "The Draft of the Guidance of Accepting the Overseas Clinical Trial Data for Medical Device", which is applicable to medical devices (including in vitro diagnostic reagents, IVDs).