• 2020-02-14 03:58:45

In order to optimize the evaluation system of medical device and encourage the innovation of medical equipment, the Ministry of Justice of China has drafted some changes on Regulation on the Supervision and Administration of Medical Devices. This draft is open for public comments until July 24.

• 2020-02-13 06:11:12

In order for clients to understand the key factors affecting the registration situation of medical devices in China in the last three years (2015-2017), Qualtech has provided an overview and analysis of the medical device registration data (as provided in the following sections of this article),

• 2020-02-14 04:07:23

The annual and well-known event is taken place twice a year in Ho Chi Minh City in August and Hanoi City in December, respectively. Vietnam Medi Pharm Expo has been organized for fifteen years in promoting trade activities of the pharmacy and medical equipment, strengthening local and foreign business to business operations.

• 2020-02-12 16:02:17

Health Sciences Authority (HSA) published the list of new fees applicable to health products including Medical devices, on last August 1, 2018.

• 2020-02-14 07:39:50

The Department of Industrial Policy and Promotion, Ministry of Commerce and Industry, Government of India has recently issued guidelines for implementation of Public Procurement Order No. 17 (PPO) in an aim to mandate procuring entities to make local suppliers as their priority purchase preference for medical devices,

• 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 07:51:46

The regulatory body for medical devices is Division of Medical Devices and Cosmetics under Taiwan Food and Drug Administration (TFDA). The important legal rules that govern Medical Device Affairs are the Pharmaceutical Affairs Act and the Regulations for Governing the Management of Medical Device.

• 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 06:19:28

The Medical Device Authority (MDA) is inviting all its customers to participate in a Customer Satisfaction Survey. MDA is always trying to improve quality of service provided to all its customers.

• 2020-02-15 06:47:59

Medical Tourism in Southeast Asia: Indonesia's Opportunity Cost. (n.d.). Retrieved July 28, 2017