Page 73 - 2023 Taiwan Food and Drug Administration Annual Report
P. 73
Improving Management
of Medical Devices
and Cosmetics
To implement various systems under of product information files for cosmetics and
the “Medical Devices Act”; to respond to the establish the system for Good Manufacturing
technological and innovative development Practice (GMP) so as to build a high-quality
of medical devices; and to improve the total environment for the use of cosmetics. In
life cycle management system for medical addition, a variety of test and verification
devices, TFDA has announced multiple review methods for multiple medical devices and
guidances related to the management of cosmetics have been prepared to boost the test
medical devices; launched the e-submission level and to ensure the quality and safety of
system for the registration and market approval medical devices and cosmetics.
of medical devices; improved the consultation
and support mechanism for businesses; and Section 1
reinforced the Quality Management System
(QMS) of medical devices. Advancement
of Regulations
Regarding international collaboration, Governing Medical
Taiwan took part in meetings of various Devices
international organizations, including the
Asia Pacific Economic Cooperation (APEC), ▍ Introduction of the Policy
Global Harmonization Working Party
(GHWP), and International Cooperation on Considering the rapid advancement of
Cosmetics Regulation (ICCR). Taiwan also medical devices, TFDA has been making
worked hard to secure opportunities to host efforts to boost its managerial efficacy by
important international meetings and events in expediting the harmonization of Taiwan's
order to expand the international engagement regulations with frequently updated
and influence of Taiwan.
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Regarding the management of cosmetics,
TFDA continues to promote the production
