Page 98 - 2017食品藥物管理署年報(英文版)

2017 Taiwan Food and Drug Administration Annual Report

period, 3 of them were asked to supply related documents and 2 of them

were asked to be enrolled for safety surveillance.
(C) In 2016, TFDA convened 3 cosmetics hygiene management advisory board
meetings to discuss 9 themes and assist TFDA revise “Table of cosmetics
types and scopes”, establish “Safety guidelines of cosmetics for children
use”, “Technical Guidelines for Cosmetics UVA Sunscreen Performance
Tests (Human Subject Test)” and “Technical Guidelines for Cosmetics
Sunscreen Performance Tests (Human Subject Test)”

D. Cultivate talents for risk assessments

(A) To help medical institution staffs effectively control the causes of medical
device defects and their application experience and understand correct
handling approaches, processes and provisions, TFDA hosts 8 educational
training course and 2 safety seminars in 2016. TFDA also hosts “Competitions
simulating the handling of medical device defects” and implements trial
“Accreditation reward systems of ADRs in medical institutes”.
(B) Through project counseling seed hospitals to establish nosocomial medical

device ADR system, the number of participating seed hospitals has increased
to 32 by the end of 2016.
(C) To enhance the professional knowledge and capacities of cosmetics
management in staffs of health competent authorities, TFDA held 2 seminars
in 2016. Additionally, to strengthen the awareness of Cosmetics ADR
(PAE) reporting system in general consumers and thus increase reporting
rates, TFDA organized 4 cosmetics ADR (PAE) seminars and practices in
northern, central and southern Taiwan in 2016. At the same time, through
biotechnological beauty and cosmetics exhibitions, country-tour of minibus

and the distribution of small gifts by local health bureaus, TFDA promotes
“Post-market Quality Management System for Food, Medicinal products and
Cosmetics” to enhance the reporting rate of cosmetic ADR(PAE).

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