• 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.

• 2019-11-15 02:57:23

The Ministry of Industrial Policy and Promotion, the Ministry of Commerce and Industry, and the Indian government have recently issued Public Purchase Order No. 17 in order to force procurement entities to use local suppliers as the priority procurement preference for medical equipment, as well as other products and services related to the pharmaceutical sector. (PPO) guidelines.

• 2020-02-14 14:55:31

In line with the rapid development of cloud computing, big data and artificial intelligence, mobile technology has been widely used in medical devices. Recently, China Food and Drug Administration (CFDA) released “Guidelines of Mobile Medical Device Registration." The provisions of this guideline was implemented from its effective date on December 29th, 2017.

• 2020-02-14 14:50:54

On November 16th of 2017, Philippine Food and Drug Administration (FDA) announced that the importation and exportation of radiation devices that can be ionizing and non-ionizing shall not be allowed to enter the country unless a Clearance for Customs Release (CFCR) has been issued by the Center for Device Regulation,

• 2020-02-15 06:31:28

HSA has finalized the Guidelines for Telehealth Products. Telehealth products refer to "instruments, apparatus, machines or software involved in the provision of healthcare services over physically separate environments via information communication technologies."