• 2022-12-27 08:57:20

The Center for Medical Device Evaluation (CMDE) has issued the “List of Mandatory Standards Applicable to Medical Devices” for applicants to determine the mandatory standards which apply to a specific product.

• 2022-12-27 07:25:52

On October 17th, Japan's Ministry of Health, Labor and Welfare announced an amendment in the Japanese Standard for Sterilization Validation.

• 2022-11-29 03:29:05

NMPA held a meeting to promote the implementation of the GB 9706 series standards on October 13th, 2022.

• 2022-11-29 02:56:30

Japan's Ministry of Health, Labour and Welfare announced that Japan's standard for medical device usability engineering (JIS T 62366-1) has been amended.

• 2022-08-30 02:35:39

18 medical device industry standards have been approved and are now published. The number, name, scope of standards and date of implementation can be found in the attachment.

• 2021-06-25 12:45:15

According to FDA Modernization Act, FDA publishes a series of recognized consensus standards modifications. FDA believes these modifications are closer to modern requirements for medical devices to ensure public benefit improvement. The medical device manufacturers should notice the standards change to avoid the FDA challenge.

• 2020-12-24 10:54:11

Thai FDA has recently announced a list of standards to be complied by disposable surgical masks, upon making a set of COVID-19 related medical devices announcement.

• 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 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.

• 2020-06-16 06:31:23

Ministry of Public Health Announcement regarding the Standard of Medical Device that Manufacturer or Importer must Comply 2020, is one of the countless Thai FDA Regulatory updates in June. Manufacturer and Importer may refer to this announcement as collection of guidance which standard of listed Medical Device can be denote to.