• 2020-07-31 10:15:03

In order to effectively control Medical Device and in accordance with International Medical Device Control have agreed to classified Contact Lens Care Products as Notified Medical Device.

• 2020-05-05 09:22:34

Seeking for the public comment for 3 three months, ThaiFDA amended “the Draft of the Product Containing Alcohol for Humans and Animals Sterilization” on several points, including the scope of the guideline, the verification report and labelling etc.

• 2020-02-14 07:39:04

The Government of India, Ministry of Health and Family Welfare has released guidelines with respect to Grouping of Medical Devices for applicants who intend to apply for a license to import or manufacture medical devices for sale and distribution in India.

• 2019-11-15 03:00:54

The Government of India and the Ministry of Health and Welfare have issued guidelines for the grouping of medical devices on the wish to apply for a license to import or manufacture medical devices for sale and distribution in India.

• 2020-02-14 07:47:14

In order to create favorable conditions for importers, the customs office shall handle the goods release procedures for special-purpose medical equipment and instruments, shall apply 5% VAT on the basis of written commitments and shall take responsibility before the law for the declaration.

• 2020-02-14 14:47:05

Indonesia's Ministry of Health (MoH) has enacted a new regulation, Permenkes No. 62 Year 2017, concerning Marketing Authorization of Medical Devices, In Vitro Diagnostic Medical Devices and Household Health Supplies on January 13, 2018.

• 2020-02-14 15:21:19

Head of Indonesia Ministry of Health, Nila Moeloek, said that the Ministry is trying to accelerate medical device and household products licensing by developing Single Submission and Indonesia Single Risk Management (ISRM) system. By using this system, hope the time consumed for licensing process can be accelerated,

• 2020-09-15 06:58:50

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.