• 2020-10-28 02:13:28

It is our great honor to invite Dr. Wei-Jen Chang, a professor from the school of Dentistry at Taipei Medical University, to speak at the Digital Dental Implant Workshop, which will be held from 2020/11/11 (Wed) to 2020/11/14 (Sat) 09:00-17:30 (GMT+8).

• 2020-10-21 01:42:37

Food and Drug Administration urgently announced certain control measures for powdered surgical gloves regarding the technical issues of the powder used in manufacturing process which may cause serious adverse effect to end-users or patients.

• 2020-10-19 09:48:24

Food and Drug Administration has announced sets of documentation required for Licensed Medical Device Manufacturing / Import License Renewal and Notified Medical Device Manufacturing / Import License Renewal that will expire in December 31st, 2020.

• 2020-10-19 09:39:21

Since MDR/IVDR will not automatically apply in UK from 1 January 2021, MHRA has published a new guidance document related to how medical devices will be regulated in the Great Britain after that. According to the guidance, CE marking/certification will be valid until 30 June 2023 for the Great Britain market.

• 2020-09-15 08:58:35

Thailand’s Ministry of Public Health has announced the medical devices that are exempted form compliance with certain control measures under Section 6 (18) of the Medical Device Act B.E. 2551.

• 2020-09-15 08:54:58

Ministry of Public Health has made an announcement regarding the Declaration Form for Importer to declare when import all the listed medical device that comply with the standards in 2020.

• 2020-09-15 08:44:25

Thailand’s Ministry of Public Health has announced a set of medical device definition for manufacturers and importers to follow when registering their medical device according to risk-based classification, to gradually endorse the transition of Thailand away from policy-based classification.

• 2020-09-15 06:53:41

Ministry of Public Health has made 2 additional announcements regarding the Standards of Medical Device that manufacturer or importer must comply to in 2020.

• 2020-09-15 06:35:40

MDCG has published a guidance for notified bodies on the use of MDASP audit reports in surveillance audit carried out under MDR/IVDR. For those with similar or equivalent requirements, positive QMS conformity result might lead to a reduction of the focus on covered aspect.

• 2020-08-13 02:35:55

TFDA is now collecting comments and suggestions for the drafting of “Regulations Governing Delegation or Commission of Medical Devices Test” (collecting deadline: 2020/09/07). This article presents a closer look of this upcoming regulation.