• 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 07:50:54

The Unique Device Identification (UDI) system is a set of alphanumeric codes that serves to enhance monitoring activities for medical devices. It consists two parts: (1) UDI (an array of alphanumeric codes) and (2) UDI carrier which come in three distinct types: (a) QR code, (b) Bar code, or (c) RFID/NFC.

• 2020-02-14 07:50:05

The applicant may initiate the cancellation of the registration license of imported medical equipment to CFDA. This administrative application will not charge any application fee. The applicant shall prepare the submission documents to cancel the application. The CFDA will conduct a formal review on the cancellation application.

• 2020-02-14 07:49:21

This major announcement was made by the Department’s Halal Hub Division director, Datuk Sirajuddin Suhaimee in early February 2018, who said the certification, drafted together with the Department of Standards Malaysia, was now at the final stage of public feedback.

• 2020-02-14 07:48:41

The Medical Device Authority (MDA) of Malaysia has organised for a medical device exhibition to be held in Malaysia in April 2018. This event, the Malaysia Medical Device Expo, is an initiative by MDA to bring light to latest innovative technologies and advances of global medical devices, in hopes to provide all its stakeholders a one-stop centre for medical devices solutions.

• 2020-02-14 07:47:54

The Guidelines released by the Department of Health concerning Medical Device Registration is in place to be officiated following its publication. This shall be implemented a year after its effective date. Delayed implementation allows sufficient preparation for applicants in securing technical documents crucial to the registration process.

• 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 07:46:31

With its immense dedication to level up the dental profession, the Asia Pacific Dental Congress, together with the Philippine Dental Association, holds its 40th Annual Convention on 7 - 11 May 2018 with its chosen theme "Intensifying professionalism in synergy with dental science and technology" at the SMX Convention Center Manila.

• 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.